Name: rs506128
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.

rs506128

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:226514599 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.225576 (68203/302350, ALFA)
G=0.196237 (51942/264690, TOPMED)
G=0.198847 (27357/137578, GnomAD) (+ 20 more)
G=0.18808 (14802/78700, PAGE_STUDY)
G=0.22689 (6411/28256, 14KJPN)
G=0.22906 (3839/16760, 8.3KJPN)
G=0.1838 (1177/6404, 1000G_30x)
G=0.1819 (911/5008, 1000G)
G=0.2042 (915/4480, Estonian)
G=0.2470 (952/3854, ALSPAC)
G=0.2171 (805/3708, TWINSUK)
G=0.2587 (758/2930, KOREAN)
G=0.2078 (433/2084, HGDP_Stanford)
G=0.1638 (310/1892, HapMap)
G=0.2331 (427/1832, Korea1K)
G=0.240 (240/998, GoNL)
G=0.256 (202/790, PRJEB37584)
G=0.348 (209/600, NorthernSweden)
G=0.175 (92/526, SGDP_PRJ)
G=0.292 (63/216, Qatari)
G=0.12 (7/56, Siberian)
G=0.28 (11/40, GENOME_DK)
G=0.19 (6/32, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	307386	G=0.225062	A=0.774938	0.051564	0.601439	0.346997	3
European	Sub	270532	G=0.228712	A=0.771288	0.052482	0.595057	0.352461	0
African	Sub	9526	G=0.1083	A=0.8917	0.011127	0.794457	0.194415	0
African Others	Sub	372	G=0.062	A=0.938	0.005376	0.88172	0.112903	0
African American	Sub	9154	G=0.1102	A=0.8898	0.011361	0.790911	0.197728	0
Asian	Sub	3934	G=0.2811	A=0.7189	0.074733	0.512456	0.412811	1
East Asian	Sub	3188	G=0.2613	A=0.7387	0.062108	0.539523	0.398369	1
Other Asian	Sub	746	G=0.366	A=0.634	0.128686	0.396783	0.474531	0
Latin American 1	Sub	1134	G=0.2063	A=0.7937	0.051146	0.638448	0.310406	1
Latin American 2	Sub	7224	G=0.2576	A=0.7424	0.068383	0.553156	0.378461	0
South Asian	Sub	5224	G=0.1524	A=0.8476	0.031011	0.726263	0.242726	6
Other	Sub	9812	G=0.2322	A=0.7678	0.054831	0.590501	0.354668	0

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	302350	G=0.225576	A=0.774424
Allele Frequency Aggregator	European	Sub	267438	G=0.228737	A=0.771263
Allele Frequency Aggregator	Other	Sub	9012	G=0.2348	A=0.7652
Allele Frequency Aggregator	African	Sub	8384	G=0.1094	A=0.8906
Allele Frequency Aggregator	Latin American 2	Sub	7224	G=0.2576	A=0.7424
Allele Frequency Aggregator	South Asian	Sub	5224	G=0.1524	A=0.8476
Allele Frequency Aggregator	Asian	Sub	3934	G=0.2811	A=0.7189
Allele Frequency Aggregator	Latin American 1	Sub	1134	G=0.2063	A=0.7937
TopMed	Global	Study-wide	264690	G=0.196237	A=0.803763
gnomAD - Genomes	Global	Study-wide	137578	G=0.198847	A=0.801153
gnomAD - Genomes	European	Sub	74716	G=0.23283	A=0.76717
gnomAD - Genomes	African	Sub	41038	G=0.11195	A=0.88805
gnomAD - Genomes	American	Sub	13260	G=0.24925	A=0.75075
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.2324	A=0.7676
gnomAD - Genomes	East Asian	Sub	3108	G=0.2773	A=0.7227
gnomAD - Genomes	Other	Sub	2134	G=0.2006	A=0.7994
The PAGE Study	Global	Study-wide	78700	G=0.18808	A=0.81192
The PAGE Study	AfricanAmerican	Sub	32516	G=0.11407	A=0.88593
The PAGE Study	Mexican	Sub	10810	G=0.25273	A=0.74727
The PAGE Study	Asian	Sub	8318	G=0.2332	A=0.7668
The PAGE Study	PuertoRican	Sub	7916	G=0.1998	A=0.8002
The PAGE Study	NativeHawaiian	Sub	4534	G=0.3805	A=0.6195
The PAGE Study	Cuban	Sub	4230	G=0.2142	A=0.7858
The PAGE Study	Dominican	Sub	3828	G=0.1855	A=0.8145
The PAGE Study	CentralAmerican	Sub	2450	G=0.2494	A=0.7506
The PAGE Study	SouthAmerican	Sub	1982	G=0.2699	A=0.7301
The PAGE Study	NativeAmerican	Sub	1260	G=0.1905	A=0.8095
The PAGE Study	SouthAsian	Sub	856	G=0.131	A=0.869
14KJPN	JAPANESE	Study-wide	28256	G=0.22689	A=0.77311
8.3KJPN	JAPANESE	Study-wide	16760	G=0.22906	A=0.77094
1000Genomes_30x	Global	Study-wide	6404	G=0.1838	A=0.8162
1000Genomes_30x	African	Sub	1786	G=0.0924	A=0.9076
1000Genomes_30x	Europe	Sub	1266	G=0.2306	A=0.7694
1000Genomes_30x	South Asian	Sub	1202	G=0.1348	A=0.8652
1000Genomes_30x	East Asian	Sub	1170	G=0.2667	A=0.7333
1000Genomes_30x	American	Sub	980	G=0.251	A=0.749
1000Genomes	Global	Study-wide	5008	G=0.1819	A=0.8181
1000Genomes	African	Sub	1322	G=0.0923	A=0.9077
1000Genomes	East Asian	Sub	1008	G=0.2609	A=0.7391
1000Genomes	Europe	Sub	1006	G=0.2276	A=0.7724
1000Genomes	South Asian	Sub	978	G=0.127	A=0.873
1000Genomes	American	Sub	694	G=0.249	A=0.751
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.2042	A=0.7958
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.2470	A=0.7530
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.2171	A=0.7829
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.2587	A=0.7413
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.2078	A=0.7922
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.272	A=0.728
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.196	A=0.804
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.160	A=0.840
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.212	A=0.787
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.095	A=0.905
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.269	A=0.731
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.26	A=0.74
HapMap	Global	Study-wide	1892	G=0.1638	A=0.8362
HapMap	American	Sub	770	G=0.201	A=0.799
HapMap	African	Sub	692	G=0.079	A=0.921
HapMap	Asian	Sub	254	G=0.244	A=0.756
HapMap	Europe	Sub	176	G=0.216	A=0.784
Korean Genome Project	KOREAN	Study-wide	1832	G=0.2331	A=0.7669
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.240	A=0.760
CNV burdens in cranial meningiomas	Global	Study-wide	790	G=0.256	A=0.744
CNV burdens in cranial meningiomas	CRM	Sub	790	G=0.256	A=0.744
Northern Sweden	ACPOP	Study-wide	600	G=0.348	A=0.652
SGDP_PRJ	Global	Study-wide	526	G=0.175	A=0.825
Qatari	Global	Study-wide	216	G=0.292	A=0.708
Siberian	Global	Study-wide	56	G=0.12	A=0.88
The Danish reference pan genome	Danish	Study-wide	40	G=0.28	A=0.72
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	32	G=0.19	A=0.81

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 1	NC_000001.11:g.226514599G>A
GRCh37.p13 chr 1	NC_000001.10:g.226702300G>A

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	G=	A
GRCh38.p14 chr 1	NC_000001.11:g.226514599=	NC_000001.11:g.226514599G>A
GRCh37.p13 chr 1	NC_000001.10:g.226702300=	NC_000001.10:g.226702300G>A

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#.

139 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss676178	Aug 11, 2000 (83)
2	SC_JCM	ss2624524	Nov 08, 2000 (89)
3	BCM_SSAHASNP	ss9825288	Jul 11, 2003 (116)
4	WI_SSAHASNP	ss11357048	Jul 11, 2003 (116)
5	ABI	ss43997630	Mar 15, 2006 (126)
6	ILLUMINA	ss67410936	Nov 30, 2006 (127)
7	ILLUMINA	ss67775959	Nov 30, 2006 (127)
8	ILLUMINA	ss68242686	Dec 12, 2006 (127)
9	PERLEGEN	ss68795091	May 17, 2007 (127)
10	ILLUMINA	ss70842254	May 27, 2008 (130)
11	ILLUMINA	ss71426329	May 17, 2007 (127)
12	ILLUMINA	ss75441554	Dec 06, 2007 (129)
13	HGSV	ss81751222	Dec 16, 2007 (130)
14	KRIBB_YJKIM	ss83469507	Dec 16, 2007 (130)
15	BCMHGSC_JDW	ss87993918	Mar 23, 2008 (129)
16	HUMANGENOME_JCVI	ss99292690	Feb 06, 2009 (130)
17	BGI	ss102827965	Feb 23, 2009 (131)
18	1000GENOMES	ss108999917	Jan 23, 2009 (130)
19	1000GENOMES	ss111870300	Jan 25, 2009 (130)
20	ILLUMINA-UK	ss119229981	Dec 01, 2009 (131)
21	ENSEMBL	ss144346647	Dec 01, 2009 (131)
22	ILLUMINA	ss154335698	Dec 01, 2009 (131)
23	ILLUMINA	ss159512294	Dec 01, 2009 (131)
24	ILLUMINA	ss160737771	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss165304010	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss165861385	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss167544235	Jul 04, 2010 (132)
28	ILLUMINA	ss173908514	Jul 04, 2010 (132)
29	BUSHMAN	ss199690143	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss205362302	Jul 04, 2010 (132)
31	1000GENOMES	ss218916569	Jul 14, 2010 (132)
32	1000GENOMES	ss230929296	Jul 14, 2010 (132)
33	1000GENOMES	ss238537012	Jul 15, 2010 (132)
34	BL	ss253868436	May 09, 2011 (134)
35	GMI	ss276244592	May 04, 2012 (137)
36	GMI	ss284240858	Apr 25, 2013 (138)
37	PJP	ss290747487	May 09, 2011 (134)
38	ILLUMINA	ss481131406	May 04, 2012 (137)
39	ILLUMINA	ss481153433	May 04, 2012 (137)
40	ILLUMINA	ss482142969	Sep 08, 2015 (146)
41	ILLUMINA	ss485360725	May 04, 2012 (137)
42	ILLUMINA	ss537305115	Sep 08, 2015 (146)
43	TISHKOFF	ss555179538	Apr 25, 2013 (138)
44	SSMP	ss648751276	Apr 25, 2013 (138)
45	ILLUMINA	ss778928032	Sep 08, 2015 (146)
46	ILLUMINA	ss783126049	Sep 08, 2015 (146)
47	ILLUMINA	ss784082659	Sep 08, 2015 (146)
48	ILLUMINA	ss832384891	Sep 08, 2015 (146)
49	ILLUMINA	ss833023598	Jul 12, 2019 (153)
50	ILLUMINA	ss834389540	Sep 08, 2015 (146)
51	EVA-GONL	ss976214793	Aug 21, 2014 (142)
52	JMKIDD_LAB	ss1068654688	Aug 21, 2014 (142)
53	1000GENOMES	ss1294915549	Aug 21, 2014 (142)
54	DDI	ss1426131817	Apr 01, 2015 (144)
55	EVA_GENOME_DK	ss1574722591	Apr 01, 2015 (144)
56	EVA_DECODE	ss1585612619	Apr 01, 2015 (144)
57	EVA_UK10K_ALSPAC	ss1602281404	Apr 01, 2015 (144)
58	EVA_UK10K_TWINSUK	ss1645275437	Apr 01, 2015 (144)
59	EVA_SVP	ss1712410510	Apr 01, 2015 (144)
60	ILLUMINA	ss1751902373	Sep 08, 2015 (146)
61	HAMMER_LAB	ss1795819745	Sep 08, 2015 (146)
62	WEILL_CORNELL_DGM	ss1919436740	Feb 12, 2016 (147)
63	ILLUMINA	ss1946025245	Feb 12, 2016 (147)
64	ILLUMINA	ss1958362817	Feb 12, 2016 (147)
65	GENOMED	ss1966989590	Jul 19, 2016 (147)
66	JJLAB	ss2020242862	Sep 14, 2016 (149)
67	USC_VALOUEV	ss2148277231	Dec 20, 2016 (150)
68	HUMAN_LONGEVITY	ss2170636587	Dec 20, 2016 (150)
69	SYSTEMSBIOZJU	ss2624632802	Nov 08, 2017 (151)
70	ILLUMINA	ss2632637764	Nov 08, 2017 (151)
71	GRF	ss2698275486	Nov 08, 2017 (151)
72	ILLUMINA	ss2710696147	Nov 08, 2017 (151)
73	GNOMAD	ss2766975369	Nov 08, 2017 (151)
74	SWEGEN	ss2988560928	Nov 08, 2017 (151)
75	ILLUMINA	ss3021186606	Nov 08, 2017 (151)
76	BIOINF_KMB_FNS_UNIBA	ss3023881905	Nov 08, 2017 (151)
77	CSHL	ss3343943461	Nov 08, 2017 (151)
78	ILLUMINA	ss3625565119	Oct 11, 2018 (152)
79	ILLUMINA	ss3626323610	Oct 11, 2018 (152)
80	ILLUMINA	ss3630667162	Oct 11, 2018 (152)
81	ILLUMINA	ss3632927949	Oct 11, 2018 (152)
82	ILLUMINA	ss3633624087	Oct 11, 2018 (152)
83	ILLUMINA	ss3634376233	Oct 11, 2018 (152)
84	ILLUMINA	ss3635317137	Oct 11, 2018 (152)
85	ILLUMINA	ss3636055111	Oct 11, 2018 (152)
86	ILLUMINA	ss3637067687	Oct 11, 2018 (152)
87	ILLUMINA	ss3637817972	Oct 11, 2018 (152)
88	ILLUMINA	ss3638924110	Oct 11, 2018 (152)
89	ILLUMINA	ss3639773773	Oct 11, 2018 (152)
90	ILLUMINA	ss3640083586	Oct 11, 2018 (152)
91	ILLUMINA	ss3640993485	Oct 11, 2018 (152)
92	ILLUMINA	ss3641287621	Oct 11, 2018 (152)
93	ILLUMINA	ss3642824051	Oct 11, 2018 (152)
94	ILLUMINA	ss3643826890	Oct 11, 2018 (152)
95	ILLUMINA	ss3644521242	Oct 11, 2018 (152)
96	URBANLAB	ss3646901842	Oct 11, 2018 (152)
97	ILLUMINA	ss3651532131	Oct 11, 2018 (152)
98	EGCUT_WGS	ss3656520019	Jul 12, 2019 (153)
99	EVA_DECODE	ss3688760304	Jul 12, 2019 (153)
100	ILLUMINA	ss3725111480	Jul 12, 2019 (153)
101	ACPOP	ss3727920849	Jul 12, 2019 (153)
102	ILLUMINA	ss3744061767	Jul 12, 2019 (153)
103	ILLUMINA	ss3744677086	Jul 12, 2019 (153)
104	EVA	ss3747418648	Jul 12, 2019 (153)
105	PAGE_CC	ss3770876467	Jul 12, 2019 (153)
106	ILLUMINA	ss3772177978	Jul 12, 2019 (153)
107	PACBIO	ss3783706175	Jul 12, 2019 (153)
108	PACBIO	ss3789315295	Jul 12, 2019 (153)
109	PACBIO	ss3794187716	Jul 12, 2019 (153)
110	KHV_HUMAN_GENOMES	ss3800421409	Jul 12, 2019 (153)
111	EVA	ss3826678589	Apr 25, 2020 (154)
112	EVA	ss3836741421	Apr 25, 2020 (154)
113	EVA	ss3842153690	Apr 25, 2020 (154)
114	HGDP	ss3847365614	Apr 25, 2020 (154)
115	SGDP_PRJ	ss3851036482	Apr 25, 2020 (154)
116	KRGDB	ss3896373642	Apr 25, 2020 (154)
117	KOGIC	ss3946628788	Apr 25, 2020 (154)
118	EVA	ss3984473100	Apr 25, 2021 (155)
119	EVA	ss3984856140	Apr 25, 2021 (155)
120	EVA	ss4016965828	Apr 25, 2021 (155)
121	TOPMED	ss4485927934	Apr 25, 2021 (155)
122	TOMMO_GENOMICS	ss5148739156	Apr 25, 2021 (155)
123	1000G_HIGH_COVERAGE	ss5246028887	Oct 12, 2022 (156)
124	EVA	ss5314687509	Oct 12, 2022 (156)
125	EVA	ss5325215029	Oct 12, 2022 (156)
126	HUGCELL_USP	ss5446440836	Oct 12, 2022 (156)
127	EVA	ss5506212799	Oct 12, 2022 (156)
128	1000G_HIGH_COVERAGE	ss5520244414	Oct 12, 2022 (156)
129	SANFORD_IMAGENETICS	ss5624231724	Oct 12, 2022 (156)
130	SANFORD_IMAGENETICS	ss5627578919	Oct 12, 2022 (156)
131	TOMMO_GENOMICS	ss5676586974	Oct 12, 2022 (156)
132	EVA	ss5799513721	Oct 12, 2022 (156)
133	YY_MCH	ss5801698447	Oct 12, 2022 (156)
134	EVA	ss5833356309	Oct 12, 2022 (156)
135	EVA	ss5847175717	Oct 12, 2022 (156)
136	EVA	ss5849315288	Oct 12, 2022 (156)
137	EVA	ss5912239969	Oct 12, 2022 (156)
138	EVA	ss5939423154	Oct 12, 2022 (156)
139	EVA	ss5979307140	Oct 12, 2022 (156)
140	1000Genomes	NC_000001.10 - 226702300	Oct 11, 2018 (152)
141	1000Genomes_30x	NC_000001.11 - 226514599	Oct 12, 2022 (156)
142	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 226702300	Oct 11, 2018 (152)
143	Genetic variation in the Estonian population	NC_000001.10 - 226702300	Oct 11, 2018 (152)
144	The Danish reference pan genome	NC_000001.10 - 226702300	Apr 25, 2020 (154)
145	gnomAD - Genomes	NC_000001.11 - 226514599	Apr 25, 2021 (155)
146	Genome of the Netherlands Release 5	NC_000001.10 - 226702300	Apr 25, 2020 (154)
147	HGDP-CEPH-db Supplement 1	NC_000001.9 - 224768923	Apr 25, 2020 (154)
148	HapMap	NC_000001.11 - 226514599	Apr 25, 2020 (154)
149	KOREAN population from KRGDB	NC_000001.10 - 226702300	Apr 25, 2020 (154)
150	Korean Genome Project	NC_000001.11 - 226514599	Apr 25, 2020 (154)
151	Northern Sweden	NC_000001.10 - 226702300	Jul 12, 2019 (153)
152	The PAGE Study	NC_000001.11 - 226514599	Jul 12, 2019 (153)
153	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 226702300	Apr 25, 2021 (155)
154	CNV burdens in cranial meningiomas	NC_000001.10 - 226702300	Apr 25, 2021 (155)
155	Qatari	NC_000001.10 - 226702300	Apr 25, 2020 (154)
156	SGDP_PRJ	NC_000001.10 - 226702300	Apr 25, 2020 (154)
157	Siberian	NC_000001.10 - 226702300	Apr 25, 2020 (154)
158	8.3KJPN	NC_000001.10 - 226702300	Apr 25, 2021 (155)
159	14KJPN	NC_000001.11 - 226514599	Oct 12, 2022 (156)
160	TopMed	NC_000001.11 - 226514599	Apr 25, 2021 (155)
161	UK 10K study - Twins	NC_000001.10 - 226702300	Oct 11, 2018 (152)
162	ALFA	NC_000001.11 - 226514599	Apr 25, 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)
rs61553522	May 27, 2008 (130)
rs74229328	Dec 02, 2009 (131)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81751222, ss3638924110, ss3639773773, ss3643826890	NC_000001.8:223009034:G:A	NC_000001.11:226514598:G:A	(self)
43506, ss87993918, ss108999917, ss111870300, ss119229981, ss165304010, ss165861385, ss167544235, ss199690143, ss205362302, ss253868436, ss276244592, ss284240858, ss290747487, ss481131406, ss1585612619, ss1712410510, ss3642824051, ss3847365614	NC_000001.9:224768922:G:A	NC_000001.11:226514598:G:A	(self)
5779759, 3194498, 2258267, 1913582, 1396091, 3551036, 1205714, 82067, 22421, 1478670, 3053462, 793585, 6708463, 3194498, ss218916569, ss230929296, ss238537012, ss481153433, ss482142969, ss485360725, ss537305115, ss555179538, ss648751276, ss778928032, ss783126049, ss784082659, ss832384891, ss833023598, ss834389540, ss976214793, ss1068654688, ss1294915549, ss1426131817, ss1574722591, ss1602281404, ss1645275437, ss1751902373, ss1795819745, ss1919436740, ss1946025245, ss1958362817, ss1966989590, ss2020242862, ss2148277231, ss2624632802, ss2632637764, ss2698275486, ss2710696147, ss2766975369, ss2988560928, ss3021186606, ss3343943461, ss3625565119, ss3626323610, ss3630667162, ss3632927949, ss3633624087, ss3634376233, ss3635317137, ss3636055111, ss3637067687, ss3637817972, ss3640083586, ss3640993485, ss3641287621, ss3644521242, ss3651532131, ss3656520019, ss3727920849, ss3744061767, ss3744677086, ss3747418648, ss3772177978, ss3783706175, ss3789315295, ss3794187716, ss3826678589, ss3836741421, ss3851036482, ss3896373642, ss3984473100, ss3984856140, ss4016965828, ss5148739156, ss5314687509, ss5325215029, ss5506212799, ss5624231724, ss5627578919, ss5799513721, ss5833356309, ss5847175717, ss5939423154, ss5979307140	NC_000001.10:226702299:G:A	NC_000001.11:226514598:G:A	(self)
7770349, 41511513, 282379, 3006789, 97936, 10424078, 49534269, 12935141698, ss2170636587, ss3023881905, ss3646901842, ss3688760304, ss3725111480, ss3770876467, ss3800421409, ss3842153690, ss3946628788, ss4485927934, ss5246028887, ss5446440836, ss5520244414, ss5676586974, ss5801698447, ss5849315288, ss5912239969	NC_000001.11:226514598:G:A	NC_000001.11:226514598:G:A	(self)
ss9825288, ss11357048	NT_004559.10:215617:G:A	NC_000001.11:226514598:G:A	(self)
ss676178, ss2624524, ss43997630, ss67410936, ss67775959, ss68242686, ss68795091, ss70842254, ss71426329, ss75441554, ss83469507, ss99292690, ss102827965, ss144346647, ss154335698, ss159512294, ss160737771, ss173908514	NT_167186.1:20220078:G:A	NC_000001.11:226514598:G:A	(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 rs506128

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

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Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs506128