Name: rs2006776
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs2006776

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:54837267 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.189100 (57283/302924, ALFA)
G=0.222313 (58844/264690, TOPMED)
G=0.220270 (30833/139978, GnomAD) (+ 20 more)
G=0.23009 (18108/78700, PAGE_STUDY)
G=0.06883 (1945/28258, 14KJPN)
G=0.06653 (1115/16760, 8.3KJPN)
G=0.2203 (1411/6404, 1000G_30x)
G=0.2171 (1087/5008, 1000G)
G=0.1960 (878/4480, Estonian)
G=0.1762 (679/3854, ALSPAC)
G=0.2031 (753/3708, TWINSUK)
G=0.0802 (235/2930, KOREAN)
G=0.1742 (363/2084, HGDP_Stanford)
G=0.2354 (445/1890, HapMap)
G=0.225 (225/998, GoNL)
G=0.096 (76/788, PRJEB37584)
G=0.227 (136/600, NorthernSweden)
G=0.190 (41/216, Qatari)
G=0.065 (14/214, Vietnamese)
A=0.426 (80/188, SGDP_PRJ)
G=0.25 (10/40, GENOME_DK)
A=0.50 (10/20, Siberian)
G=0.50 (10/20, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAB27B : Intron Variant
Publications: 1 citation
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	307960	A=0.810514	G=0.189486
European	Sub	271890	A=0.814910	G=0.185090
African	Sub	8912	A=0.6823	G=0.3177
African Others	Sub	372	A=0.712	G=0.288
African American	Sub	8540	A=0.6810	G=0.3190
Asian	Sub	3938	A=0.9005	G=0.0995
East Asian	Sub	3192	A=0.9129	G=0.0871
Other Asian	Sub	746	A=0.847	G=0.153
Latin American 1	Sub	1132	A=0.8180	G=0.1820
Latin American 2	Sub	7194	A=0.8019	G=0.1981
South Asian	Sub	5222	A=0.7518	G=0.2482
Other	Sub	9672	A=0.8056	G=0.1944

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	302924	A=0.810900	G=0.189100
Allele Frequency Aggregator	European	Sub	268796	A=0.814960	G=0.185040
Allele Frequency Aggregator	Other	Sub	8872	A=0.8044	G=0.1956
Allele Frequency Aggregator	African	Sub	7770	A=0.6794	G=0.3206
Allele Frequency Aggregator	Latin American 2	Sub	7194	A=0.8019	G=0.1981
Allele Frequency Aggregator	South Asian	Sub	5222	A=0.7518	G=0.2482
Allele Frequency Aggregator	Asian	Sub	3938	A=0.9005	G=0.0995
Allele Frequency Aggregator	Latin American 1	Sub	1132	A=0.8180	G=0.1820
TopMed	Global	Study-wide	264690	A=0.777687	G=0.222313
gnomAD - Genomes	Global	Study-wide	139978	A=0.779730	G=0.220270
gnomAD - Genomes	European	Sub	75846	A=0.81903	G=0.18097
gnomAD - Genomes	African	Sub	41916	A=0.68344	G=0.31656
gnomAD - Genomes	American	Sub	13614	A=0.81379	G=0.18621
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.8098	G=0.1902
gnomAD - Genomes	East Asian	Sub	3130	A=0.9179	G=0.0821
gnomAD - Genomes	Other	Sub	2150	A=0.8074	G=0.1926
The PAGE Study	Global	Study-wide	78700	A=0.76991	G=0.23009
The PAGE Study	AfricanAmerican	Sub	32516	A=0.68858	G=0.31142
The PAGE Study	Mexican	Sub	10808	A=0.79071	G=0.20929
The PAGE Study	Asian	Sub	8318	A=0.9241	G=0.0759
The PAGE Study	PuertoRican	Sub	7918	A=0.8114	G=0.1886
The PAGE Study	NativeHawaiian	Sub	4534	A=0.9230	G=0.0770
The PAGE Study	Cuban	Sub	4230	A=0.7979	G=0.2021
The PAGE Study	Dominican	Sub	3828	A=0.7398	G=0.2602
The PAGE Study	CentralAmerican	Sub	2450	A=0.7771	G=0.2229
The PAGE Study	SouthAmerican	Sub	1982	A=0.8158	G=0.1842
The PAGE Study	NativeAmerican	Sub	1260	A=0.8111	G=0.1889
The PAGE Study	SouthAsian	Sub	856	A=0.711	G=0.289
14KJPN	JAPANESE	Study-wide	28258	A=0.93117	G=0.06883
8.3KJPN	JAPANESE	Study-wide	16760	A=0.93347	G=0.06653
1000Genomes_30x	Global	Study-wide	6404	A=0.7797	G=0.2203
1000Genomes_30x	African	Sub	1786	A=0.6837	G=0.3163
1000Genomes_30x	Europe	Sub	1266	A=0.8191	G=0.1809
1000Genomes_30x	South Asian	Sub	1202	A=0.7230	G=0.2770
1000Genomes_30x	East Asian	Sub	1170	A=0.9299	G=0.0701
1000Genomes_30x	American	Sub	980	A=0.794	G=0.206
1000Genomes	Global	Study-wide	5008	A=0.7829	G=0.2171
1000Genomes	African	Sub	1322	A=0.6823	G=0.3177
1000Genomes	East Asian	Sub	1008	A=0.9315	G=0.0685
1000Genomes	Europe	Sub	1006	A=0.8151	G=0.1849
1000Genomes	South Asian	Sub	978	A=0.718	G=0.282
1000Genomes	American	Sub	694	A=0.804	G=0.196
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8040	G=0.1960
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8238	G=0.1762
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.7969	G=0.2031
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.9198	G=0.0802
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.8258	G=0.1742
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.917	G=0.083
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.732	G=0.268
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.837	G=0.163
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.859	G=0.141
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.773	G=0.227
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.833	G=0.167
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.72	G=0.28
HapMap	Global	Study-wide	1890	A=0.7646	G=0.2354
HapMap	American	Sub	770	A=0.766	G=0.234
HapMap	African	Sub	690	A=0.704	G=0.296
HapMap	Asian	Sub	254	A=0.913	G=0.087
HapMap	Europe	Sub	176	A=0.778	G=0.222
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.775	G=0.225
CNV burdens in cranial meningiomas	Global	Study-wide	788	A=0.904	G=0.096
CNV burdens in cranial meningiomas	CRM	Sub	788	A=0.904	G=0.096
Northern Sweden	ACPOP	Study-wide	600	A=0.773	G=0.227
Qatari	Global	Study-wide	216	A=0.810	G=0.190
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.935	G=0.065
SGDP_PRJ	Global	Study-wide	188	A=0.426	G=0.574
The Danish reference pan genome	Danish	Study-wide	40	A=0.75	G=0.25
Siberian	Global	Study-wide	20	A=0.50	G=0.50

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 18	NC_000018.10:g.54837267A>G
GRCh37.p13 chr 18	NC_000018.9:g.52504498A>G

Gene: RAB27B, RAB27B, member RAS oncogene family (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAB27B transcript variant 2	NM_001375327.1:c.-19-4030… NM_001375327.1:c.-19-40300A>G	N/A	Intron Variant
RAB27B transcript variant 1	NM_004163.4:c.-20+8567A>G	N/A	Intron Variant
RAB27B transcript variant X7	XM_006722518.2:c.-20+8567… XM_006722518.2:c.-20+8567A>G	N/A	Intron Variant
RAB27B transcript variant X2	XM_017025913.2:c.-224+856… XM_017025913.2:c.-224+8567A>G	N/A	Intron Variant
RAB27B transcript variant X5	XM_017025914.2:c.-223-247… XM_017025914.2:c.-223-24753A>G	N/A	Intron Variant
RAB27B transcript variant X1	XM_047437725.1:c.-20+8567… XM_047437725.1:c.-20+8567A>G	N/A	Intron Variant
RAB27B transcript variant X3	XM_047437726.1:c.-19-4030… XM_047437726.1:c.-19-40300A>G	N/A	Intron Variant
RAB27B transcript variant X6	XM_024451232.2:c.	N/A	Genic Upstream Transcript Variant
RAB27B transcript variant X4	XR_007066208.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	A=	G
GRCh38.p14 chr 18	NC_000018.10:g.54837267=	NC_000018.10:g.54837267A>G
GRCh37.p13 chr 18	NC_000018.9:g.52504498=	NC_000018.9:g.52504498A>G
RAB27B transcript variant 2	NM_001375327.1:c.-19-40300=	NM_001375327.1:c.-19-40300A>G
RAB27B transcript variant 1	NM_004163.4:c.-20+8567=	NM_004163.4:c.-20+8567A>G
RAB27B transcript variant X2	XM_005266733.1:c.-19-40300=	XM_005266733.1:c.-19-40300A>G
RAB27B transcript variant X7	XM_006722518.2:c.-20+8567=	XM_006722518.2:c.-20+8567A>G
RAB27B transcript variant X2	XM_017025913.2:c.-224+8567=	XM_017025913.2:c.-224+8567A>G
RAB27B transcript variant X5	XM_017025914.2:c.-223-24753=	XM_017025914.2:c.-223-24753A>G
RAB27B transcript variant X1	XM_047437725.1:c.-20+8567=	XM_047437725.1:c.-20+8567A>G
RAB27B transcript variant X3	XM_047437726.1:c.-19-40300=	XM_047437726.1:c.-19-40300A>G

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

122 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2892152	Jan 23, 2001 (92)
2	CSHL-HAPMAP	ss16769362	Feb 27, 2004 (120)
3	ABI	ss44144314	Mar 13, 2006 (126)
4	PERLEGEN	ss46554193	Mar 13, 2006 (126)
5	AFFY	ss65942732	Dec 01, 2006 (127)
6	ILLUMINA	ss66579122	Dec 01, 2006 (127)
7	ILLUMINA	ss67214770	Dec 01, 2006 (127)
8	ILLUMINA	ss67608382	Dec 01, 2006 (127)
9	PERLEGEN	ss69215303	May 18, 2007 (127)
10	ILLUMINA	ss70693028	May 24, 2008 (130)
11	ILLUMINA	ss71258251	May 18, 2007 (127)
12	ILLUMINA	ss74930419	Dec 06, 2007 (129)
13	ILLUMINA	ss79106983	Dec 14, 2007 (130)
14	KRIBB_YJKIM	ss83942703	Dec 14, 2007 (130)
15	HGSV	ss85050247	Dec 14, 2007 (130)
16	ILLUMINA-UK	ss117887488	Feb 14, 2009 (130)
17	ILLUMINA	ss121882015	Dec 01, 2009 (131)
18	ILLUMINA	ss153812926	Dec 01, 2009 (131)
19	GMI	ss155214497	Dec 01, 2009 (131)
20	ILLUMINA	ss159348355	Dec 01, 2009 (131)
21	ILLUMINA	ss160487638	Dec 01, 2009 (131)
22	ENSEMBL	ss161858024	Dec 01, 2009 (131)
23	ILLUMINA	ss170941322	Jul 04, 2010 (132)
24	ILLUMINA	ss173040166	Jul 04, 2010 (132)
25	BUSHMAN	ss203311149	Jul 04, 2010 (132)
26	1000GENOMES	ss227887356	Jul 14, 2010 (132)
27	1000GENOMES	ss237486871	Jul 15, 2010 (132)
28	1000GENOMES	ss243732041	Jul 15, 2010 (132)
29	GMI	ss283009471	May 04, 2012 (137)
30	ILLUMINA	ss480378413	May 04, 2012 (137)
31	ILLUMINA	ss480390856	May 04, 2012 (137)
32	ILLUMINA	ss481166008	Sep 08, 2015 (146)
33	ILLUMINA	ss484986788	May 04, 2012 (137)
34	ILLUMINA	ss537021777	Sep 08, 2015 (146)
35	TISHKOFF	ss565672680	Apr 25, 2013 (138)
36	SSMP	ss661508038	Apr 25, 2013 (138)
37	ILLUMINA	ss778849778	Aug 21, 2014 (142)
38	ILLUMINA	ss782939709	Aug 21, 2014 (142)
39	ILLUMINA	ss783902326	Aug 21, 2014 (142)
40	ILLUMINA	ss825437501	Jul 19, 2016 (147)
41	ILLUMINA	ss832195291	Apr 01, 2015 (144)
42	ILLUMINA	ss832860298	Aug 21, 2014 (142)
43	ILLUMINA	ss833451128	Aug 21, 2014 (142)
44	ILLUMINA	ss834310423	Aug 21, 2014 (142)
45	EVA-GONL	ss993781981	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1081540251	Aug 21, 2014 (142)
47	1000GENOMES	ss1361233930	Aug 21, 2014 (142)
48	DDI	ss1428234106	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1578426302	Apr 01, 2015 (144)
50	EVA_UK10K_ALSPAC	ss1636988410	Apr 01, 2015 (144)
51	EVA_UK10K_TWINSUK	ss1679982443	Apr 01, 2015 (144)
52	EVA_DECODE	ss1697843587	Apr 01, 2015 (144)
53	EVA_SVP	ss1713629927	Apr 01, 2015 (144)
54	ILLUMINA	ss1752260091	Sep 08, 2015 (146)
55	HAMMER_LAB	ss1809073639	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1937249948	Feb 12, 2016 (147)
57	ILLUMINA	ss1946504903	Feb 12, 2016 (147)
58	ILLUMINA	ss1959808010	Feb 12, 2016 (147)
59	GENOMED	ss1968536128	Jul 19, 2016 (147)
60	JJLAB	ss2029394963	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2157902121	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2222005694	Dec 20, 2016 (150)
63	ILLUMINA	ss2633479098	Nov 08, 2017 (151)
64	GRF	ss2702492683	Nov 08, 2017 (151)
65	ILLUMINA	ss2710869608	Nov 08, 2017 (151)
66	GNOMAD	ss2957272729	Nov 08, 2017 (151)
67	SWEGEN	ss3016610947	Nov 08, 2017 (151)
68	ILLUMINA	ss3021847653	Nov 08, 2017 (151)
69	BIOINF_KMB_FNS_UNIBA	ss3028527015	Nov 08, 2017 (151)
70	CSHL	ss3352047243	Nov 08, 2017 (151)
71	ILLUMINA	ss3625726399	Oct 12, 2018 (152)
72	ILLUMINA	ss3627820615	Oct 12, 2018 (152)
73	ILLUMINA	ss3631455450	Oct 12, 2018 (152)
74	ILLUMINA	ss3633164308	Oct 12, 2018 (152)
75	ILLUMINA	ss3633873162	Oct 12, 2018 (152)
76	ILLUMINA	ss3634708214	Oct 12, 2018 (152)
77	ILLUMINA	ss3635560407	Oct 12, 2018 (152)
78	ILLUMINA	ss3636397659	Oct 12, 2018 (152)
79	ILLUMINA	ss3637312024	Oct 12, 2018 (152)
80	ILLUMINA	ss3638198919	Oct 12, 2018 (152)
81	ILLUMINA	ss3639107630	Oct 12, 2018 (152)
82	ILLUMINA	ss3639562648	Oct 12, 2018 (152)
83	ILLUMINA	ss3640415522	Oct 12, 2018 (152)
84	ILLUMINA	ss3643174431	Oct 12, 2018 (152)
85	ILLUMINA	ss3644706980	Oct 12, 2018 (152)
86	ILLUMINA	ss3652269779	Oct 12, 2018 (152)
87	EGCUT_WGS	ss3683456084	Jul 13, 2019 (153)
88	EVA_DECODE	ss3701762087	Jul 13, 2019 (153)
89	ILLUMINA	ss3725680693	Jul 13, 2019 (153)
90	ACPOP	ss3742588680	Jul 13, 2019 (153)
91	ILLUMINA	ss3744159463	Jul 13, 2019 (153)
92	ILLUMINA	ss3745008356	Jul 13, 2019 (153)
93	EVA	ss3755455947	Jul 13, 2019 (153)
94	PAGE_CC	ss3771974790	Jul 13, 2019 (153)
95	ILLUMINA	ss3772505825	Jul 13, 2019 (153)
96	PACBIO	ss3788385385	Jul 13, 2019 (153)
97	PACBIO	ss3793314782	Jul 13, 2019 (153)
98	PACBIO	ss3798201217	Jul 13, 2019 (153)
99	KHV_HUMAN_GENOMES	ss3820712956	Jul 13, 2019 (153)
100	EVA	ss3835195828	Apr 27, 2020 (154)
101	HGDP	ss3847585155	Apr 27, 2020 (154)
102	SGDP_PRJ	ss3887126739	Apr 27, 2020 (154)
103	KRGDB	ss3937010684	Apr 27, 2020 (154)
104	EVA	ss3984733614	Apr 26, 2021 (155)
105	EVA	ss4017800787	Apr 26, 2021 (155)
106	TOPMED	ss5058538861	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5225404847	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5305473402	Oct 16, 2022 (156)
109	EVA	ss5315936981	Oct 16, 2022 (156)
110	EVA	ss5431755109	Oct 16, 2022 (156)
111	HUGCELL_USP	ss5498223324	Oct 16, 2022 (156)
112	EVA	ss5511959330	Oct 16, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5610410971	Oct 16, 2022 (156)
114	SANFORD_IMAGENETICS	ss5661398352	Oct 16, 2022 (156)
115	TOMMO_GENOMICS	ss5783263218	Oct 16, 2022 (156)
116	EVA	ss5799994942	Oct 16, 2022 (156)
117	YY_MCH	ss5817144376	Oct 16, 2022 (156)
118	EVA	ss5827616093	Oct 16, 2022 (156)
119	EVA	ss5847823074	Oct 16, 2022 (156)
120	EVA	ss5852075339	Oct 16, 2022 (156)
121	EVA	ss5874294026	Oct 16, 2022 (156)
122	EVA	ss5952819408	Oct 16, 2022 (156)
123	1000Genomes	NC_000018.9 - 52504498	Oct 12, 2018 (152)
124	1000Genomes_30x	NC_000018.10 - 54837267	Oct 16, 2022 (156)
125	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 52504498	Oct 12, 2018 (152)
126	Genetic variation in the Estonian population	NC_000018.9 - 52504498	Oct 12, 2018 (152)
127	The Danish reference pan genome	NC_000018.9 - 52504498	Apr 27, 2020 (154)
128	gnomAD - Genomes	NC_000018.10 - 54837267	Apr 26, 2021 (155)
129	Genome of the Netherlands Release 5	NC_000018.9 - 52504498	Apr 27, 2020 (154)
130	HGDP-CEPH-db Supplement 1	NC_000018.8 - 50655496	Apr 27, 2020 (154)
131	HapMap	NC_000018.10 - 54837267	Apr 27, 2020 (154)
132	KOREAN population from KRGDB	NC_000018.9 - 52504498	Apr 27, 2020 (154)
133	Northern Sweden	NC_000018.9 - 52504498	Jul 13, 2019 (153)
134	The PAGE Study	NC_000018.10 - 54837267	Jul 13, 2019 (153)
135	CNV burdens in cranial meningiomas	NC_000018.9 - 52504498	Apr 26, 2021 (155)
136	Qatari	NC_000018.9 - 52504498	Apr 27, 2020 (154)
137	SGDP_PRJ	NC_000018.9 - 52504498	Apr 27, 2020 (154)
138	Siberian	NC_000018.9 - 52504498	Apr 27, 2020 (154)
139	8.3KJPN	NC_000018.9 - 52504498	Apr 26, 2021 (155)
140	14KJPN	NC_000018.10 - 54837267	Oct 16, 2022 (156)
141	TopMed	NC_000018.10 - 54837267	Apr 26, 2021 (155)
142	UK 10K study - Twins	NC_000018.9 - 52504498	Oct 12, 2018 (152)
143	A Vietnamese Genetic Variation Database	NC_000018.9 - 52504498	Jul 13, 2019 (153)
144	ALFA	NC_000018.10 - 54837267	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs57707004	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
263047, ss85050247, ss117887488, ss160487638, ss203311149, ss283009471, ss480378413, ss825437501, ss1697843587, ss1713629927, ss3639107630, ss3639562648, ss3643174431, ss3847585155	NC_000018.8:50655495:A:G	NC_000018.10:54837266:A:G	(self)
74570153, 41322634, 29194332, 4617402, 18408593, 44188078, 15873545, 283166, 19291870, 39143719, 10418475, 83374154, 41322634, 9130345, ss227887356, ss237486871, ss243732041, ss480390856, ss481166008, ss484986788, ss537021777, ss565672680, ss661508038, ss778849778, ss782939709, ss783902326, ss832195291, ss832860298, ss833451128, ss834310423, ss993781981, ss1081540251, ss1361233930, ss1428234106, ss1578426302, ss1636988410, ss1679982443, ss1752260091, ss1809073639, ss1937249948, ss1946504903, ss1959808010, ss1968536128, ss2029394963, ss2157902121, ss2633479098, ss2702492683, ss2710869608, ss2957272729, ss3016610947, ss3021847653, ss3352047243, ss3625726399, ss3627820615, ss3631455450, ss3633164308, ss3633873162, ss3634708214, ss3635560407, ss3636397659, ss3637312024, ss3638198919, ss3640415522, ss3644706980, ss3652269779, ss3683456084, ss3742588680, ss3744159463, ss3745008356, ss3755455947, ss3772505825, ss3788385385, ss3793314782, ss3798201217, ss3835195828, ss3887126739, ss3937010684, ss3984733614, ss4017800787, ss5225404847, ss5315936981, ss5431755109, ss5511959330, ss5661398352, ss5799994942, ss5827616093, ss5847823074, ss5952819408	NC_000018.9:52504497:A:G	NC_000018.10:54837266:A:G	(self)
97936906, 526038908, 1612734, 1196259, 117100322, 274084524, 4978442645, ss2222005694, ss3028527015, ss3701762087, ss3725680693, ss3771974790, ss3820712956, ss5058538861, ss5305473402, ss5498223324, ss5610410971, ss5783263218, ss5817144376, ss5852075339, ss5874294026	NC_000018.10:54837266:A:G	NC_000018.10:54837266:A:G	(self)
ss16769362	NT_025028.13:295361:A:G	NC_000018.10:54837266:A:G	(self)
ss2892152, ss44144314, ss46554193, ss65942732, ss66579122, ss67214770, ss67608382, ss69215303, ss70693028, ss71258251, ss74930419, ss79106983, ss83942703, ss121882015, ss153812926, ss155214497, ss159348355, ss161858024, ss170941322, ss173040166	NT_025028.14:295361:A:G	NC_000018.10:54837266:A:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs2006776

PMID	Title	Author	Year	Journal
19156173	Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.	Amin N et al.	2009	European journal of human genetics

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2006776