Name: rs1851378
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.

rs1851378

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:160795732 (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>A / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.443130 (117292/264690, TOPMED)
G=0.422588 (59159/139992, GnomAD)
G=0.36912 (29155/78986, ALFA) (+ 19 more)
T=0.31595 (8928/28258, 14KJPN)
T=0.31211 (5231/16760, 8.3KJPN)
G=0.4808 (3079/6404, 1000G_30x)
G=0.4862 (2435/5008, 1000G)
G=0.3254 (1458/4480, Estonian)
G=0.3373 (1300/3854, ALSPAC)
G=0.3363 (1247/3708, TWINSUK)
T=0.3594 (1053/2930, KOREAN)
G=0.4760 (991/2082, HGDP_Stanford)
T=0.3390 (621/1832, Korea1K)
T=0.4817 (527/1094, HapMap)
G=0.309 (308/998, GoNL)
G=0.380 (228/600, NorthernSweden)
T=0.303 (120/396, SGDP_PRJ)
G=0.315 (68/216, Qatari)
T=0.454 (98/216, Vietnamese)
G=0.42 (17/40, GENOME_DK)
T=0.35 (14/40, Siberian)
G=0.12 (2/16, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPM1L : Intron Variant
Publications: 0 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	78986	T=0.63088	G=0.36912
European	Sub	62620	T=0.65934	G=0.34066
African	Sub	5208	T=0.4291	G=0.5709
African Others	Sub	182	T=0.385	G=0.615
African American	Sub	5026	T=0.4308	G=0.5692
Asian	Sub	240	T=0.429	G=0.571
East Asian	Sub	166	T=0.349	G=0.651
Other Asian	Sub	74	T=0.61	G=0.39
Latin American 1	Sub	398	T=0.570	G=0.430
Latin American 2	Sub	3390	T=0.5035	G=0.4965
South Asian	Sub	4970	T=0.6082	G=0.3918
Other	Sub	2160	T=0.5778	G=0.4222

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=0.556870	G=0.443130
gnomAD - Genomes	Global	Study-wide	139992	T=0.577412	G=0.422588
gnomAD - Genomes	European	Sub	75860	T=0.66559	G=0.33441
gnomAD - Genomes	African	Sub	41904	T=0.42836	G=0.57164
gnomAD - Genomes	American	Sub	13638	T=0.55507	G=0.44493
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.6787	G=0.3213
gnomAD - Genomes	East Asian	Sub	3118	T=0.4173	G=0.5827
gnomAD - Genomes	Other	Sub	2148	T=0.5885	G=0.4115
Allele Frequency Aggregator	Total	Global	78986	T=0.63088	G=0.36912
Allele Frequency Aggregator	European	Sub	62620	T=0.65934	G=0.34066
Allele Frequency Aggregator	African	Sub	5208	T=0.4291	G=0.5709
Allele Frequency Aggregator	South Asian	Sub	4970	T=0.6082	G=0.3918
Allele Frequency Aggregator	Latin American 2	Sub	3390	T=0.5035	G=0.4965
Allele Frequency Aggregator	Other	Sub	2160	T=0.5778	G=0.4222
Allele Frequency Aggregator	Latin American 1	Sub	398	T=0.570	G=0.430
Allele Frequency Aggregator	Asian	Sub	240	T=0.429	G=0.571
14KJPN	JAPANESE	Study-wide	28258	T=0.31595	G=0.68405
8.3KJPN	JAPANESE	Study-wide	16760	T=0.31211	G=0.68789
1000Genomes_30x	Global	Study-wide	6404	T=0.5192	G=0.4808
1000Genomes_30x	African	Sub	1786	T=0.4239	G=0.5761
1000Genomes_30x	Europe	Sub	1266	T=0.6643	G=0.3357
1000Genomes_30x	South Asian	Sub	1202	T=0.6339	G=0.3661
1000Genomes_30x	East Asian	Sub	1170	T=0.4120	G=0.5880
1000Genomes_30x	American	Sub	980	T=0.493	G=0.507
1000Genomes	Global	Study-wide	5008	T=0.5138	G=0.4862
1000Genomes	African	Sub	1322	T=0.4175	G=0.5825
1000Genomes	East Asian	Sub	1008	T=0.4117	G=0.5883
1000Genomes	Europe	Sub	1006	T=0.6660	G=0.3340
1000Genomes	South Asian	Sub	978	T=0.611	G=0.389
1000Genomes	American	Sub	694	T=0.487	G=0.513
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6746	G=0.3254
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6627	G=0.3373
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6637	G=0.3363
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3594	A=0.0000, G=0.6406
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.5240	G=0.4760
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	468	T=0.391	G=0.609
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.539	G=0.461
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.631	G=0.369
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.631	G=0.369
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.525	G=0.475
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.296	G=0.704
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.99	G=0.01
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3390	G=0.6610
HapMap	Global	Study-wide	1094	T=0.4817	G=0.5183
HapMap	American	Sub	544	T=0.483	G=0.517
HapMap	Asian	Sub	254	T=0.382	G=0.618
HapMap	Europe	Sub	176	T=0.716	G=0.284
HapMap	African	Sub	120	T=0.342	G=0.658
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.691	G=0.309
Northern Sweden	ACPOP	Study-wide	600	T=0.620	G=0.380
SGDP_PRJ	Global	Study-wide	396	T=0.303	G=0.697
Qatari	Global	Study-wide	216	T=0.685	G=0.315
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.454	G=0.546
The Danish reference pan genome	Danish	Study-wide	40	T=0.57	G=0.42
Siberian	Global	Study-wide	40	T=0.35	G=0.65
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	16	T=0.88	G=0.12

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 3	NC_000003.12:g.160795732T>A
GRCh38.p14 chr 3	NC_000003.12:g.160795732T>G
GRCh37.p13 chr 3	NC_000003.11:g.160513520T>A
GRCh37.p13 chr 3	NC_000003.11:g.160513520T>G

Gene: PPM1L, protein phosphatase, Mg2+/Mn2+ dependent 1L (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPM1L transcript variant 1	NM_139245.4:c.399+39025T>A	N/A	Intron Variant
PPM1L transcript variant 2	NM_001317911.2:c.	N/A	Genic Upstream Transcript Variant
PPM1L transcript variant 3	NM_001317912.2:c.	N/A	Genic Upstream Transcript Variant
PPM1L transcript variant 4	NR_134243.2:n.	N/A	Genic Upstream Transcript Variant
PPM1L transcript variant X1	XM_011512440.4:c.399+3902… XM_011512440.4:c.399+39025T>A	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	T=	A	G
GRCh38.p14 chr 3	NC_000003.12:g.160795732=	NC_000003.12:g.160795732T>A	NC_000003.12:g.160795732T>G
GRCh37.p13 chr 3	NC_000003.11:g.160513520=	NC_000003.11:g.160513520T>A	NC_000003.11:g.160513520T>G
PPM1L transcript	NM_139245.2:c.399+39025=	NM_139245.2:c.399+39025T>A	NM_139245.2:c.399+39025T>G
PPM1L transcript variant 1	NM_139245.4:c.399+39025=	NM_139245.4:c.399+39025T>A	NM_139245.4:c.399+39025T>G
PPM1L transcript variant X1	XM_011512440.4:c.399+39025=	XM_011512440.4:c.399+39025T>A	XM_011512440.4:c.399+39025T>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#.

98 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2723576	Jan 12, 2001 (92)
2	WI_SSAHASNP	ss11555692	Jul 11, 2003 (116)
3	BCM_SSAHASNP	ss14165072	Dec 05, 2003 (119)
4	CSHL-HAPMAP	ss16935976	Feb 27, 2004 (120)
5	CSHL-HAPMAP	ss17725119	Feb 27, 2004 (120)
6	SSAHASNP	ss21876110	Apr 05, 2004 (121)
7	PERLEGEN	ss24221155	Sep 20, 2004 (123)
8	ABI	ss44373712	Mar 14, 2006 (126)
9	AFFY	ss66201712	Nov 30, 2006 (127)
10	ILLUMINA	ss66773060	Nov 30, 2006 (127)
11	ILLUMINA	ss67199341	Nov 30, 2006 (127)
12	ILLUMINA	ss67591033	Nov 30, 2006 (127)
13	ILLUMINA	ss70677556	May 25, 2008 (130)
14	ILLUMINA	ss71240868	May 17, 2007 (127)
15	ILLUMINA	ss75770128	Dec 06, 2007 (129)
16	AFFY	ss76290073	Dec 06, 2007 (129)
17	ILLUMINA	ss79095871	Dec 15, 2007 (130)
18	KRIBB_YJKIM	ss83886128	Dec 15, 2007 (130)
19	HGSV	ss84624636	Dec 15, 2007 (130)
20	BCMHGSC_JDW	ss92347501	Mar 24, 2008 (129)
21	HUMANGENOME_JCVI	ss96068540	Feb 05, 2009 (130)
22	1000GENOMES	ss111231064	Jan 25, 2009 (130)
23	ILLUMINA	ss121823248	Dec 01, 2009 (131)
24	ENSEMBL	ss133155061	Dec 01, 2009 (131)
25	ENSEMBL	ss139258002	Dec 01, 2009 (131)
26	ILLUMINA	ss153748033	Dec 01, 2009 (131)
27	GMI	ss156420069	Dec 01, 2009 (131)
28	ILLUMINA	ss159332327	Dec 01, 2009 (131)
29	COMPLETE_GENOMICS	ss164777018	Jul 04, 2010 (132)
30	COMPLETE_GENOMICS	ss167380265	Jul 04, 2010 (132)
31	ILLUMINA	ss170832554	Jul 04, 2010 (132)
32	ILLUMINA	ss172941862	Jul 04, 2010 (132)
33	AFFY	ss173141028	Jul 04, 2010 (132)
34	BUSHMAN	ss203436290	Jul 04, 2010 (132)
35	1000GENOMES	ss220537017	Jul 14, 2010 (132)
36	1000GENOMES	ss232111571	Jul 14, 2010 (132)
37	1000GENOMES	ss239466000	Jul 15, 2010 (132)
38	BL	ss253639680	May 09, 2011 (134)
39	GMI	ss277426441	May 04, 2012 (137)
40	PJP	ss292959415	May 09, 2011 (134)
41	ILLUMINA	ss536996644	Sep 08, 2015 (146)
42	TISHKOFF	ss557070801	Apr 25, 2013 (138)
43	SSMP	ss650808128	Apr 25, 2013 (138)
44	ILLUMINA	ss825426389	Apr 01, 2015 (144)
45	ILLUMINA	ss832844326	Jul 13, 2019 (153)
46	EVA-GONL	ss979373860	Aug 21, 2014 (142)
47	JMKIDD_LAB	ss1070992437	Aug 21, 2014 (142)
48	1000GENOMES	ss1306972508	Aug 21, 2014 (142)
49	DDI	ss1429647787	Apr 01, 2015 (144)
50	EVA_GENOME_DK	ss1580264229	Apr 01, 2015 (144)
51	EVA_DECODE	ss1588866578	Apr 01, 2015 (144)
52	EVA_UK10K_ALSPAC	ss1608646648	Apr 01, 2015 (144)
53	EVA_UK10K_TWINSUK	ss1651640681	Apr 01, 2015 (144)
54	EVA_SVP	ss1712626861	Apr 01, 2015 (144)
55	HAMMER_LAB	ss1800324592	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1922597088	Feb 12, 2016 (147)
57	GENOMED	ss1969570118	Jul 19, 2016 (147)
58	JJLAB	ss2021871200	Sep 14, 2016 (149)
59	USC_VALOUEV	ss2149966985	Dec 20, 2016 (150)
60	HUMAN_LONGEVITY	ss2257527132	Dec 20, 2016 (150)
61	SYSTEMSBIOZJU	ss2625436644	Nov 08, 2017 (151)
62	ILLUMINA	ss2635126956	Nov 08, 2017 (151)
63	GRF	ss2705385516	Nov 08, 2017 (151)
64	GNOMAD	ss2801465114	Nov 08, 2017 (151)
65	SWEGEN	ss2993521486	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3024702837	Nov 08, 2017 (151)
67	CSHL	ss3345359261	Nov 08, 2017 (151)
68	ILLUMINA	ss3628821126	Oct 12, 2018 (152)
69	ILLUMINA	ss3638452804	Oct 12, 2018 (152)
70	ILLUMINA	ss3639229149	Oct 12, 2018 (152)
71	ILLUMINA	ss3639633974	Oct 12, 2018 (152)
72	ILLUMINA	ss3643406835	Oct 12, 2018 (152)
73	URBANLAB	ss3647569092	Oct 12, 2018 (152)
74	EGCUT_WGS	ss3661462198	Jul 13, 2019 (153)
75	EVA_DECODE	ss3710680275	Jul 13, 2019 (153)
76	ACPOP	ss3730526498	Jul 13, 2019 (153)
77	EVA	ss3760942168	Jul 13, 2019 (153)
78	KHV_HUMAN_GENOMES	ss3804076730	Jul 13, 2019 (153)
79	EVA	ss3828176412	Apr 25, 2020 (154)
80	HGDP	ss3847730129	Apr 25, 2020 (154)
81	SGDP_PRJ	ss3857398053	Apr 25, 2020 (154)
82	KRGDB	ss3903453952	Apr 25, 2020 (154)
83	KOGIC	ss3952801740	Apr 25, 2020 (154)
84	EVA	ss3985033099	Apr 26, 2021 (155)
85	EVA	ss4017115883	Apr 26, 2021 (155)
86	TOPMED	ss4590751470	Apr 26, 2021 (155)
87	TOMMO_GENOMICS	ss5162500535	Apr 26, 2021 (155)
88	1000G_HIGH_COVERAGE	ss5256737310	Oct 12, 2022 (156)
89	HUGCELL_USP	ss5455805180	Oct 12, 2022 (156)
90	EVA	ss5507277573	Oct 12, 2022 (156)
91	1000G_HIGH_COVERAGE	ss5536546181	Oct 12, 2022 (156)
92	SANFORD_IMAGENETICS	ss5633593960	Oct 12, 2022 (156)
93	TOMMO_GENOMICS	ss5695643094	Oct 12, 2022 (156)
94	YY_MCH	ss5804423009	Oct 12, 2022 (156)
95	EVA	ss5826753651	Oct 12, 2022 (156)
96	EVA	ss5853924144	Oct 12, 2022 (156)
97	EVA	ss5871820554	Oct 12, 2022 (156)
98	EVA	ss5961963737	Oct 12, 2022 (156)
99	1000Genomes	NC_000003.11 - 160513520	Oct 12, 2018 (152)
100	1000Genomes_30x	NC_000003.12 - 160795732	Oct 12, 2022 (156)
101	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 160513520	Oct 12, 2018 (152)
102	Genetic variation in the Estonian population	NC_000003.11 - 160513520	Oct 12, 2018 (152)
103	The Danish reference pan genome	NC_000003.11 - 160513520	Apr 25, 2020 (154)
104	gnomAD - Genomes	NC_000003.12 - 160795732	Apr 26, 2021 (155)
105	Genome of the Netherlands Release 5	NC_000003.11 - 160513520	Apr 25, 2020 (154)
106	HGDP-CEPH-db Supplement 1	NC_000003.10 - 161996214	Apr 25, 2020 (154)
107	HapMap	NC_000003.12 - 160795732	Apr 25, 2020 (154)
108	KOREAN population from KRGDB	NC_000003.11 - 160513520	Apr 25, 2020 (154)
109	Korean Genome Project	NC_000003.12 - 160795732	Apr 25, 2020 (154)
110	Northern Sweden	NC_000003.11 - 160513520	Jul 13, 2019 (153)
111	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000003.11 - 160513520	Apr 26, 2021 (155)
112	Qatari	NC_000003.11 - 160513520	Apr 25, 2020 (154)
113	SGDP_PRJ	NC_000003.11 - 160513520	Apr 25, 2020 (154)
114	Siberian	NC_000003.11 - 160513520	Apr 25, 2020 (154)
115	8.3KJPN	NC_000003.11 - 160513520	Apr 26, 2021 (155)
116	14KJPN	NC_000003.12 - 160795732	Oct 12, 2022 (156)
117	TopMed	NC_000003.12 - 160795732	Apr 26, 2021 (155)
118	UK 10K study - Twins	NC_000003.11 - 160513520	Oct 12, 2018 (152)
119	A Vietnamese Genetic Variation Database	NC_000003.11 - 160513520	Jul 13, 2019 (153)
120	ALFA	NC_000003.12 - 160795732	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)
rs17217188	Oct 07, 2004 (123)
rs59313835	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10631346, ss3903453952	NC_000003.11:160513519:T:A	NC_000003.12:160795731:T:A	(self)
ss84624636, ss3639229149, ss3639633974	NC_000003.9:161996221:T:G	NC_000003.12:160795731:T:G	(self)
408021, ss66201712, ss76290073, ss92347501, ss111231064, ss164777018, ss167380265, ss173141028, ss203436290, ss253639680, ss277426441, ss292959415, ss825426389, ss1588866578, ss1712626861, ss2635126956, ss3643406835, ss3847730129	NC_000003.10:161996213:T:G	NC_000003.12:160795731:T:G	(self)
18266310, 10177744, 7200446, 6429168, 4470422, 10631346, 3811363, 259026, 4639018, 9415033, 2483339, 20469842, 10177744, 2221446, ss220537017, ss232111571, ss239466000, ss536996644, ss557070801, ss650808128, ss832844326, ss979373860, ss1070992437, ss1306972508, ss1429647787, ss1580264229, ss1608646648, ss1651640681, ss1800324592, ss1922597088, ss1969570118, ss2021871200, ss2149966985, ss2625436644, ss2705385516, ss2801465114, ss2993521486, ss3345359261, ss3628821126, ss3638452804, ss3661462198, ss3730526498, ss3760942168, ss3828176412, ss3857398053, ss3903453952, ss3985033099, ss4017115883, ss5162500535, ss5507277573, ss5633593960, ss5826753651, ss5961963737	NC_000003.11:160513519:T:G	NC_000003.12:160795731:T:G	(self)
24072116, 129754030, 2495658, 9179741, 29480198, 428129025, 2987260918, ss2257527132, ss3024702837, ss3647569092, ss3710680275, ss3804076730, ss3952801740, ss4590751470, ss5256737310, ss5455805180, ss5536546181, ss5695643094, ss5804423009, ss5853924144, ss5871820554	NC_000003.12:160795731:T:G	NC_000003.12:160795731:T:G	(self)
ss11555692	NT_005612.13:66913059:T:G	NC_000003.12:160795731:T:G	(self)
ss14165072, ss16935976, ss17725119, ss21876110	NT_005612.14:67008677:T:G	NC_000003.12:160795731:T:G	(self)
ss2723576, ss24221155, ss44373712, ss66773060, ss67199341, ss67591033, ss70677556, ss71240868, ss75770128, ss79095871, ss83886128, ss96068540, ss121823248, ss133155061, ss139258002, ss153748033, ss156420069, ss159332327, ss170832554, ss172941862	NT_005612.16:67008665:T:G	NC_000003.12:160795731:T:G	(self)

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

No publications for rs1851378

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

rs1851378