Name: rs1471225
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.

rs1471225

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:29596192 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.472300 (125013/264690, TOPMED)
T=0.478778 (78126/163178, ALFA)
C=0.480079 (67213/140004, GnomAD) (+ 19 more)
C=0.42959 (33807/78696, PAGE_STUDY)
C=0.33375 (9431/28258, 14KJPN)
C=0.33419 (5601/16760, 8.3KJPN)
C=0.4418 (2829/6404, 1000G_30x)
C=0.4385 (2196/5008, 1000G)
T=0.4848 (2172/4480, Estonian)
T=0.4574 (1763/3854, ALSPAC)
T=0.4773 (1770/3708, TWINSUK)
C=0.3618 (1060/2930, KOREAN)
T=0.481 (480/998, GoNL)
C=0.401 (316/788, PRJEB37584)
T=0.470 (282/600, NorthernSweden)
T=0.354 (131/370, SGDP_PRJ)
C=0.427 (140/328, HapMap)
C=0.495 (107/216, Qatari)
C=0.394 (85/216, Vietnamese)
T=0.35 (14/40, GENOME_DK)
T=0.26 (10/38, Siberian)
T=0.14 (2/14, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM189A1 : Intron Variant
Publications: 2 citations
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	163300	T=0.478775	C=0.521225
European	Sub	142862	T=0.465113	C=0.534887
African	Sub	4278	T=0.6019	C=0.3981
African Others	Sub	168	T=0.625	C=0.375
African American	Sub	4110	T=0.6010	C=0.3990
Asian	Sub	6204	T=0.6294	C=0.3706
East Asian	Sub	4416	T=0.6332	C=0.3668
Other Asian	Sub	1788	T=0.6202	C=0.3798
Latin American 1	Sub	442	T=0.523	C=0.477
Latin American 2	Sub	950	T=0.539	C=0.461
South Asian	Sub	276	T=0.525	C=0.475
Other	Sub	8288	T=0.5271	C=0.4729

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
TopMed	Global	Study-wide	264690	T=0.527700	C=0.472300
Allele Frequency Aggregator	Total	Global	163178	T=0.478778	C=0.521222
Allele Frequency Aggregator	European	Sub	142758	T=0.465102	C=0.534898
Allele Frequency Aggregator	Other	Sub	8284	T=0.5273	C=0.4727
Allele Frequency Aggregator	Asian	Sub	6204	T=0.6294	C=0.3706
Allele Frequency Aggregator	African	Sub	4264	T=0.6023	C=0.3977
Allele Frequency Aggregator	Latin American 2	Sub	950	T=0.539	C=0.461
Allele Frequency Aggregator	Latin American 1	Sub	442	T=0.523	C=0.477
Allele Frequency Aggregator	South Asian	Sub	276	T=0.525	C=0.475
gnomAD - Genomes	Global	Study-wide	140004	T=0.519921	C=0.480079
gnomAD - Genomes	European	Sub	75826	T=0.46405	C=0.53595
gnomAD - Genomes	African	Sub	41962	T=0.60259	C=0.39741
gnomAD - Genomes	American	Sub	13624	T=0.57311	C=0.42689
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.4461	C=0.5539
gnomAD - Genomes	East Asian	Sub	3122	T=0.6160	C=0.3840
gnomAD - Genomes	Other	Sub	2146	T=0.5144	C=0.4856
The PAGE Study	Global	Study-wide	78696	T=0.57041	C=0.42959
The PAGE Study	AfricanAmerican	Sub	32514	T=0.59833	C=0.40167
The PAGE Study	Mexican	Sub	10808	T=0.54672	C=0.45328
The PAGE Study	Asian	Sub	8318	T=0.6429	C=0.3571
The PAGE Study	PuertoRican	Sub	7918	T=0.5431	C=0.4569
The PAGE Study	NativeHawaiian	Sub	4534	T=0.4740	C=0.5260
The PAGE Study	Cuban	Sub	4230	T=0.5078	C=0.4922
The PAGE Study	Dominican	Sub	3828	T=0.5238	C=0.4762
The PAGE Study	CentralAmerican	Sub	2450	T=0.5812	C=0.4188
The PAGE Study	SouthAmerican	Sub	1982	T=0.5378	C=0.4622
The PAGE Study	NativeAmerican	Sub	1260	T=0.5040	C=0.4960
The PAGE Study	SouthAsian	Sub	854	T=0.528	C=0.472
14KJPN	JAPANESE	Study-wide	28258	T=0.66625	C=0.33375
8.3KJPN	JAPANESE	Study-wide	16760	T=0.66581	C=0.33419
1000Genomes_30x	Global	Study-wide	6404	T=0.5582	C=0.4418
1000Genomes_30x	African	Sub	1786	T=0.6041	C=0.3959
1000Genomes_30x	Europe	Sub	1266	T=0.4739	C=0.5261
1000Genomes_30x	South Asian	Sub	1202	T=0.5208	C=0.4792
1000Genomes_30x	East Asian	Sub	1170	T=0.6538	C=0.3462
1000Genomes_30x	American	Sub	980	T=0.515	C=0.485
1000Genomes	Global	Study-wide	5008	T=0.5615	C=0.4385
1000Genomes	African	Sub	1322	T=0.6082	C=0.3918
1000Genomes	East Asian	Sub	1008	T=0.6518	C=0.3482
1000Genomes	Europe	Sub	1006	T=0.4761	C=0.5239
1000Genomes	South Asian	Sub	978	T=0.522	C=0.478
1000Genomes	American	Sub	694	T=0.520	C=0.480
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4848	C=0.5152
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4574	C=0.5426
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4773	C=0.5227
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6382	C=0.3618
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.481	C=0.519
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.599	C=0.401
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.599	C=0.401
Northern Sweden	ACPOP	Study-wide	600	T=0.470	C=0.530
SGDP_PRJ	Global	Study-wide	370	T=0.354	C=0.646
HapMap	Global	Study-wide	328	T=0.573	C=0.427
HapMap	American	Sub	120	T=0.383	C=0.617
HapMap	African	Sub	118	T=0.686	C=0.314
HapMap	Asian	Sub	90	T=0.68	C=0.32
Qatari	Global	Study-wide	216	T=0.505	C=0.495
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.606	C=0.394
The Danish reference pan genome	Danish	Study-wide	40	T=0.35	C=0.65
Siberian	Global	Study-wide	38	T=0.26	C=0.74
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	14	T=0.14	C=0.86

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 15	NC_000015.10:g.29596192T>C
GRCh37.p13 chr 15	NC_000015.9:g.29888396T>C
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.1767835C>T
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.1880319C>T

Gene: FAM189A1, family with sequence similarity 189 member A1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ENTREP2 transcript variant 3	NM_001387215.1:c.-70+7890… NM_001387215.1:c.-70+78907A>G	N/A	Intron Variant
ENTREP2 transcript variant 4	NM_001387216.1:c.-70+7890… NM_001387216.1:c.-70+78907A>G	N/A	Intron Variant
ENTREP2 transcript variant 5	NM_001387217.1:c.-70+7890… NM_001387217.1:c.-70+78907A>G	N/A	Intron Variant
ENTREP2 transcript variant 2	NM_001387214.1:c.	N/A	Genic Upstream Transcript Variant
ENTREP2 transcript variant 1	NM_015307.2:c.	N/A	Genic Upstream Transcript Variant
ENTREP2 transcript variant X1	XM_011521407.3:c.	N/A	Genic Upstream Transcript Variant
ENTREP2 transcript variant X2	XM_047432323.1:c.	N/A	Genic Upstream Transcript 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	T=	C
GRCh38.p14 chr 15	NC_000015.10:g.29596192=	NC_000015.10:g.29596192T>C
GRCh37.p13 chr 15	NC_000015.9:g.29888396=	NC_000015.9:g.29888396T>C
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.1767835C>T	NW_011332701.1:g.1767835=
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.1880319C>T	NT_187660.1:g.1880319=
ENTREP2 transcript variant 3	NM_001387215.1:c.-70+78907=	NM_001387215.1:c.-70+78907A>G
ENTREP2 transcript variant 4	NM_001387216.1:c.-70+78907=	NM_001387216.1:c.-70+78907A>G
ENTREP2 transcript variant 5	NM_001387217.1:c.-70+78907=	NM_001387217.1:c.-70+78907A>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#.

97 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2292104	Oct 23, 2000 (88)
2	BCM_SSAHASNP	ss10764540	Jul 11, 2003 (116)
3	SSAHASNP	ss21233459	Apr 05, 2004 (121)
4	PERLEGEN	ss24446588	Sep 20, 2004 (123)
5	PERLEGEN	ss69171680	May 18, 2007 (127)
6	HGSV	ss77607237	Dec 06, 2007 (129)
7	HGSV	ss78453334	Dec 06, 2007 (129)
8	BCMHGSC_JDW	ss90105947	Mar 24, 2008 (129)
9	HUMANGENOME_JCVI	ss96746782	Feb 06, 2009 (130)
10	1000GENOMES	ss108701303	Jan 23, 2009 (130)
11	ILLUMINA-UK	ss118174683	Feb 14, 2009 (130)
12	ENSEMBL	ss134212717	Dec 01, 2009 (131)
13	ENSEMBL	ss136930415	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss167725703	Jul 04, 2010 (132)
15	BUSHMAN	ss200664823	Jul 04, 2010 (132)
16	BCM-HGSC-SUB	ss207234979	Jul 04, 2010 (132)
17	1000GENOMES	ss211586917	Jul 14, 2010 (132)
18	1000GENOMES	ss226817303	Jul 14, 2010 (132)
19	1000GENOMES	ss236725023	Jul 15, 2010 (132)
20	1000GENOMES	ss243122658	Jul 15, 2010 (132)
21	BL	ss254868015	May 09, 2011 (134)
22	GMI	ss282196647	May 04, 2012 (137)
23	GMI	ss286925902	Apr 25, 2013 (138)
24	PJP	ss291809529	May 09, 2011 (134)
25	EXOME_CHIP	ss491491506	May 04, 2012 (137)
26	TISHKOFF	ss564389173	Apr 25, 2013 (138)
27	SSMP	ss660102244	Apr 25, 2013 (138)
28	ILLUMINA	ss780681988	Aug 21, 2014 (142)
29	ILLUMINA	ss783355321	Aug 21, 2014 (142)
30	EVA-GONL	ss991632697	Aug 21, 2014 (142)
31	JMKIDD_LAB	ss1080009552	Aug 21, 2014 (142)
32	1000GENOMES	ss1352858800	Aug 21, 2014 (142)
33	DDI	ss1427578173	Apr 01, 2015 (144)
34	EVA_GENOME_DK	ss1577528507	Apr 01, 2015 (144)
35	EVA_UK10K_ALSPAC	ss1632685987	Apr 01, 2015 (144)
36	EVA_UK10K_TWINSUK	ss1675680020	Apr 01, 2015 (144)
37	EVA_DECODE	ss1695644022	Apr 01, 2015 (144)
38	ILLUMINA	ss1752154787	Sep 08, 2015 (146)
39	HAMMER_LAB	ss1808135877	Sep 08, 2015 (146)
40	ILLUMINA	ss1917893796	Feb 12, 2016 (147)
41	WEILL_CORNELL_DGM	ss1935033507	Feb 12, 2016 (147)
42	ILLUMINA	ss1946388686	Feb 12, 2016 (147)
43	ILLUMINA	ss1959598228	Feb 12, 2016 (147)
44	GENOMED	ss1968072498	Jul 19, 2016 (147)
45	JJLAB	ss2028295626	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2156692617	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2205580896	Dec 20, 2016 (150)
48	ILLUMINA	ss2633209515	Nov 08, 2017 (151)
49	ILLUMINA	ss2633209516	Nov 08, 2017 (151)
50	GRF	ss2701153939	Nov 08, 2017 (151)
51	AFFY	ss2985667684	Nov 08, 2017 (151)
52	SWEGEN	ss3013025908	Nov 08, 2017 (151)
53	ILLUMINA	ss3021617076	Nov 08, 2017 (151)
54	BIOINF_KMB_FNS_UNIBA	ss3027971665	Nov 08, 2017 (151)
55	CSHL	ss3351046457	Nov 08, 2017 (151)
56	ILLUMINA	ss3627324977	Oct 12, 2018 (152)
57	ILLUMINA	ss3634598301	Oct 12, 2018 (152)
58	ILLUMINA	ss3640305627	Oct 12, 2018 (152)
59	ILLUMINA	ss3644641811	Oct 12, 2018 (152)
60	URBANLAB	ss3650319287	Oct 12, 2018 (152)
61	ILLUMINA	ss3652016445	Oct 12, 2018 (152)
62	EGCUT_WGS	ss3680187825	Jul 13, 2019 (153)
63	EVA_DECODE	ss3697601590	Jul 13, 2019 (153)
64	ILLUMINA	ss3725485355	Jul 13, 2019 (153)
65	ACPOP	ss3740794917	Jul 13, 2019 (153)
66	ILLUMINA	ss3744417298	Jul 13, 2019 (153)
67	ILLUMINA	ss3744898863	Jul 13, 2019 (153)
68	EVA	ss3752901537	Jul 13, 2019 (153)
69	PAGE_CC	ss3771818910	Jul 13, 2019 (153)
70	ILLUMINA	ss3772397578	Jul 13, 2019 (153)
71	PACBIO	ss3787803616	Jul 13, 2019 (153)
72	PACBIO	ss3792822429	Jul 13, 2019 (153)
73	PACBIO	ss3797706891	Jul 13, 2019 (153)
74	KHV_HUMAN_GENOMES	ss3818219354	Jul 13, 2019 (153)
75	EVA	ss3834160722	Apr 27, 2020 (154)
76	EVA	ss3840677296	Apr 27, 2020 (154)
77	EVA	ss3846166063	Apr 27, 2020 (154)
78	SGDP_PRJ	ss3882581707	Apr 27, 2020 (154)
79	KRGDB	ss3931706605	Apr 27, 2020 (154)
80	EVA	ss3984698766	Apr 27, 2021 (155)
81	EVA	ss3985707527	Apr 27, 2021 (155)
82	VINODS	ss4032002522	Apr 27, 2021 (155)
83	TOPMED	ss4986039369	Apr 27, 2021 (155)
84	TOMMO_GENOMICS	ss5215463359	Apr 27, 2021 (155)
85	1000G_HIGH_COVERAGE	ss5297900039	Oct 17, 2022 (156)
86	EVA	ss5315772369	Oct 17, 2022 (156)
87	HUGCELL_USP	ss5491703360	Oct 17, 2022 (156)
88	EVA	ss5511384590	Oct 17, 2022 (156)
89	1000G_HIGH_COVERAGE	ss5599030324	Oct 17, 2022 (156)
90	SANFORD_IMAGENETICS	ss5624356449	Oct 17, 2022 (156)
91	SANFORD_IMAGENETICS	ss5657200186	Oct 17, 2022 (156)
92	TOMMO_GENOMICS	ss5769054345	Oct 17, 2022 (156)
93	YY_MCH	ss5815198757	Oct 17, 2022 (156)
94	EVA	ss5827996657	Oct 17, 2022 (156)
95	EVA	ss5851230872	Oct 17, 2022 (156)
96	EVA	ss5875280992	Oct 17, 2022 (156)
97	EVA	ss5948603415	Oct 17, 2022 (156)
98	1000Genomes	NC_000015.9 - 29888396	Oct 12, 2018 (152)
99	1000Genomes_30x	NC_000015.10 - 29596192	Oct 17, 2022 (156)
100	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 29888396	Oct 12, 2018 (152)
101	Genetic variation in the Estonian population	NC_000015.9 - 29888396	Oct 12, 2018 (152)
102	The Danish reference pan genome	NC_000015.9 - 29888396	Apr 27, 2020 (154)
103	gnomAD - Genomes	NC_000015.10 - 29596192	Apr 27, 2021 (155)
104	Genome of the Netherlands Release 5	NC_000015.9 - 29888396	Apr 27, 2020 (154)
105	HapMap	NC_000015.10 - 29596192	Apr 27, 2020 (154)
106	KOREAN population from KRGDB	NC_000015.9 - 29888396	Apr 27, 2020 (154)
107	Northern Sweden	NC_000015.9 - 29888396	Jul 13, 2019 (153)
108	The PAGE Study	NC_000015.10 - 29596192	Jul 13, 2019 (153)
109	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000015.9 - 29888396	Apr 27, 2021 (155)
110	CNV burdens in cranial meningiomas	NC_000015.9 - 29888396	Apr 27, 2021 (155)
111	Qatari	NC_000015.9 - 29888396	Apr 27, 2020 (154)
112	SGDP_PRJ	NC_000015.9 - 29888396	Apr 27, 2020 (154)
113	Siberian	NC_000015.9 - 29888396	Apr 27, 2020 (154)
114	8.3KJPN	NC_000015.9 - 29888396	Apr 27, 2021 (155)
115	14KJPN	NC_000015.10 - 29596192	Oct 17, 2022 (156)
116	TopMed	NC_000015.10 - 29596192	Apr 27, 2021 (155)
117	UK 10K study - Twins	NC_000015.9 - 29888396	Oct 12, 2018 (152)
118	A Vietnamese Genetic Variation Database	NC_000015.9 - 29888396	Jul 13, 2019 (153)
119	ALFA	NC_000015.10 - 29596192	Apr 27, 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)
rs17395492	Oct 08, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77607237, ss78453334, ss90105947, ss108701303, ss118174683, ss167725703, ss200664823, ss207234979, ss211586917, ss254868015, ss282196647, ss286925902, ss291809529, ss1695644022	NC_000015.8:27675687:T:C	NC_000015.10:29596191:T:C	(self)
65907331, 36591798, 25926073, 3796010, 16346049, 38883999, 14079782, 933454, 248287, 17075437, 34598687, 9208971, 73432666, 36591798, 8141512, ss226817303, ss236725023, ss243122658, ss491491506, ss564389173, ss660102244, ss780681988, ss783355321, ss991632697, ss1080009552, ss1352858800, ss1427578173, ss1577528507, ss1632685987, ss1675680020, ss1752154787, ss1808135877, ss1917893796, ss1935033507, ss1946388686, ss1959598228, ss1968072498, ss2028295626, ss2156692617, ss2633209515, ss2633209516, ss2701153939, ss2985667684, ss3013025908, ss3021617076, ss3351046457, ss3627324977, ss3634598301, ss3640305627, ss3644641811, ss3652016445, ss3680187825, ss3740794917, ss3744417298, ss3744898863, ss3752901537, ss3772397578, ss3787803616, ss3792822429, ss3797706891, ss3834160722, ss3840677296, ss3882581707, ss3931706605, ss3984698766, ss3985707527, ss5215463359, ss5315772369, ss5511384590, ss5624356449, ss5657200186, ss5827996657, ss5948603415	NC_000015.9:29888395:T:C	NC_000015.10:29596191:T:C	(self)
86556259, 464573810, 1234007, 1040379, 102891449, 201585029, 12434846165, ss2205580896, ss3027971665, ss3650319287, ss3697601590, ss3725485355, ss3771818910, ss3818219354, ss3846166063, ss4986039369, ss5297900039, ss5491703360, ss5599030324, ss5769054345, ss5815198757, ss5851230872, ss5875280992	NC_000015.10:29596191:T:C	NC_000015.10:29596191:T:C	(self)
ss10764540	NT_010194.15:678952:T:C	NC_000015.10:29596191:T:C	(self)
ss21233459	NT_010194.16:678952:T:C	NC_000015.10:29596191:T:C	(self)
ss2292104, ss24446588, ss69171680, ss96746782, ss134212717, ss136930415	NT_010194.17:678952:T:C	NC_000015.10:29596191:T:C	(self)
ss4032002522	NT_187660.1:1880318:C:C	NC_000015.10:29596191:T:C	(self)

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

2 citations for rs1471225

PMID	Title	Author	Year	Journal
19384554	Genome-wide association studies in ADHD.	Franke B et al.	2009	Human genetics
20148275	Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.	Rommelse NN et al.	2010	European child & adolescent psychiatry

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1471225