Name: rs59032726
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.

rs59032726

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:39353028-39353048 (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: del(CA)₄ / del(CA)₃ / delCACA / de…
del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.1716 (1713/9980, ALFA)
(AC)₁₀A=0.057 (43/758, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RFC1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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	9980	(AC)₁₀A=0.7351	del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0907, dupCA=0.1716, dupCACA=0.0020, dup(CA)₃=0.0006, dup(CA)₄=0.0000
Allele Frequency Aggregator	European	Sub	8186	(AC)₁₀A=0.6780	del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.1104, dupCA=0.2084, dupCACA=0.0024, dup(CA)₃=0.0007, dup(CA)₄=0.0000
Allele Frequency Aggregator	African	Sub	1222	(AC)₁₀A=1.0000	del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	252	(AC)₁₀A=1.000	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Other	Sub	198	(AC)₁₀A=0.960	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.005, dupCA=0.035, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(AC)₁₀A=1.00	del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Asian	Sub	38	(AC)₁₀A=1.00	del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(AC)₁₀A=1.00	del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
1000Genomes	Global	Study-wide	758	(AC)₁₀A=0.057	delCA=0.943
1000Genomes	East Asian	Sub	264	(AC)₁₀A=0.087	delCA=0.913
1000Genomes	Europe	Sub	210	(AC)₁₀A=0.014	delCA=0.986
1000Genomes	South Asian	Sub	146	(AC)₁₀A=0.103	delCA=0.897
1000Genomes	American	Sub	87	(AC)₁₀A=0.01	delCA=0.99
1000Genomes	African	Sub	51	(AC)₁₀A=0.02	delCA=0.98

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 4	NC_000004.12:g.39353029CA[6]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[7]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[8]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[9]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[11]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[12]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[13]
GRCh38.p14 chr 4	NC_000004.12:g.39353029CA[14]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[6]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[7]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[8]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[9]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[11]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[12]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[13]
GRCh37.p13 chr 4	NC_000004.11:g.39354649CA[14]

Gene: RFC1, replication factor C subunit 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RFC1 transcript variant 2	NM_001204747.2:c.4-1571GT… NM_001204747.2:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant 3	NM_001363495.2:c.4-1571GT… NM_001363495.2:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant 4	NM_001363496.2:c.4-1571GT… NM_001363496.2:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant 1	NM_002913.5:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant X1	XM_011513731.2:c.4-1571GT… XM_011513731.2:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant X2	XM_047416054.1:c.4-1571GT… XM_047416054.1:c.4-1571GT[6]	N/A	Intron Variant
RFC1 transcript variant X3	XR_007057951.1: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	(AC)₁₀A=	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄
GRCh38.p14 chr 4	NC_000004.12:g.39353028_39353048=	NC_000004.12:g.39353029CA[6]	NC_000004.12:g.39353029CA[7]	NC_000004.12:g.39353029CA[8]	NC_000004.12:g.39353029CA[9]	NC_000004.12:g.39353029CA[11]	NC_000004.12:g.39353029CA[12]	NC_000004.12:g.39353029CA[13]	NC_000004.12:g.39353029CA[14]
GRCh37.p13 chr 4	NC_000004.11:g.39354648_39354668=	NC_000004.11:g.39354649CA[6]	NC_000004.11:g.39354649CA[7]	NC_000004.11:g.39354649CA[8]	NC_000004.11:g.39354649CA[9]	NC_000004.11:g.39354649CA[11]	NC_000004.11:g.39354649CA[12]	NC_000004.11:g.39354649CA[13]	NC_000004.11:g.39354649CA[14]
RFC1 transcript variant 2	NM_001204747.1:c.4-1552=	NM_001204747.1:c.4-1571GT[6]	NM_001204747.1:c.4-1571GT[7]	NM_001204747.1:c.4-1571GT[8]	NM_001204747.1:c.4-1571GT[9]	NM_001204747.1:c.4-1571GT[11]	NM_001204747.1:c.4-1571GT[12]	NM_001204747.1:c.4-1571GT[13]	NM_001204747.1:c.4-1571GT[14]
RFC1 transcript variant 2	NM_001204747.2:c.4-1552=	NM_001204747.2:c.4-1571GT[6]	NM_001204747.2:c.4-1571GT[7]	NM_001204747.2:c.4-1571GT[8]	NM_001204747.2:c.4-1571GT[9]	NM_001204747.2:c.4-1571GT[11]	NM_001204747.2:c.4-1571GT[12]	NM_001204747.2:c.4-1571GT[13]	NM_001204747.2:c.4-1571GT[14]
RFC1 transcript variant 3	NM_001363495.2:c.4-1552=	NM_001363495.2:c.4-1571GT[6]	NM_001363495.2:c.4-1571GT[7]	NM_001363495.2:c.4-1571GT[8]	NM_001363495.2:c.4-1571GT[9]	NM_001363495.2:c.4-1571GT[11]	NM_001363495.2:c.4-1571GT[12]	NM_001363495.2:c.4-1571GT[13]	NM_001363495.2:c.4-1571GT[14]
RFC1 transcript variant 4	NM_001363496.2:c.4-1552=	NM_001363496.2:c.4-1571GT[6]	NM_001363496.2:c.4-1571GT[7]	NM_001363496.2:c.4-1571GT[8]	NM_001363496.2:c.4-1571GT[9]	NM_001363496.2:c.4-1571GT[11]	NM_001363496.2:c.4-1571GT[12]	NM_001363496.2:c.4-1571GT[13]	NM_001363496.2:c.4-1571GT[14]
RFC1 transcript variant 1	NM_002913.4:c.4-1552=	NM_002913.4:c.4-1571GT[6]	NM_002913.4:c.4-1571GT[7]	NM_002913.4:c.4-1571GT[8]	NM_002913.4:c.4-1571GT[9]	NM_002913.4:c.4-1571GT[11]	NM_002913.4:c.4-1571GT[12]	NM_002913.4:c.4-1571GT[13]	NM_002913.4:c.4-1571GT[14]
RFC1 transcript variant 1	NM_002913.5:c.4-1552=	NM_002913.5:c.4-1571GT[6]	NM_002913.5:c.4-1571GT[7]	NM_002913.5:c.4-1571GT[8]	NM_002913.5:c.4-1571GT[9]	NM_002913.5:c.4-1571GT[11]	NM_002913.5:c.4-1571GT[12]	NM_002913.5:c.4-1571GT[13]	NM_002913.5:c.4-1571GT[14]
RFC1 transcript variant X1	XM_005262660.1:c.4-1552=	XM_005262660.1:c.4-1571GT[6]	XM_005262660.1:c.4-1571GT[7]	XM_005262660.1:c.4-1571GT[8]	XM_005262660.1:c.4-1571GT[9]	XM_005262660.1:c.4-1571GT[11]	XM_005262660.1:c.4-1571GT[12]	XM_005262660.1:c.4-1571GT[13]	XM_005262660.1:c.4-1571GT[14]
RFC1 transcript variant X1	XM_011513731.2:c.4-1552=	XM_011513731.2:c.4-1571GT[6]	XM_011513731.2:c.4-1571GT[7]	XM_011513731.2:c.4-1571GT[8]	XM_011513731.2:c.4-1571GT[9]	XM_011513731.2:c.4-1571GT[11]	XM_011513731.2:c.4-1571GT[12]	XM_011513731.2:c.4-1571GT[13]	XM_011513731.2:c.4-1571GT[14]
RFC1 transcript variant X2	XM_047416054.1:c.4-1552=	XM_047416054.1:c.4-1571GT[6]	XM_047416054.1:c.4-1571GT[7]	XM_047416054.1:c.4-1571GT[8]	XM_047416054.1:c.4-1571GT[9]	XM_047416054.1:c.4-1571GT[11]	XM_047416054.1:c.4-1571GT[12]	XM_047416054.1:c.4-1571GT[13]	XM_047416054.1:c.4-1571GT[14]

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#.

71 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80377525	Dec 03, 2013 (138)
2	HGSV	ss81067841	Dec 04, 2013 (138)
3	HUMANGENOME_JCVI	ss95351692	Feb 13, 2009 (130)
4	GMI	ss288510239	May 04, 2012 (137)
5	1000GENOMES	ss326509091	Jan 10, 2018 (151)
6	1000GENOMES	ss326539085	Jan 10, 2018 (151)
7	1000GENOMES	ss326698713	May 09, 2011 (138)
8	LUNTER	ss551353095	Jan 10, 2018 (151)
9	LUNTER	ss551467952	Apr 25, 2013 (138)
10	LUNTER	ss553117835	Jan 10, 2018 (151)
11	SSMP	ss663507774	Jan 10, 2018 (151)
12	1000GENOMES	ss1372054897	Jan 10, 2018 (151)
13	1000GENOMES	ss1372054898	Aug 21, 2014 (142)
14	1000GENOMES	ss1372054899	Aug 21, 2014 (142)
15	DDI	ss1536403365	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1704122749	Jan 10, 2018 (151)
17	EVA_UK10K_ALSPAC	ss1704122750	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1704122769	Jan 10, 2018 (151)
19	EVA_UK10K_TWINSUK	ss1704122773	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1710142112	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1710142156	Apr 01, 2015 (144)
22	HAMMER_LAB	ss1801303927	Sep 08, 2015 (146)
23	HAMMER_LAB	ss1801303930	Sep 08, 2015 (146)
24	GENOMED	ss1969714554	Jan 10, 2018 (151)
25	SWEGEN	ss2994489840	Jan 10, 2018 (151)
26	MCHAISSO	ss3064097202	Nov 08, 2017 (151)
27	MCHAISSO	ss3064963279	Jan 10, 2018 (151)
28	MCHAISSO	ss3065944064	Nov 08, 2017 (151)
29	URBANLAB	ss3647701658	Oct 12, 2018 (152)
30	EVA_DECODE	ss3711837536	Jul 13, 2019 (153)
31	EVA_DECODE	ss3711837537	Jul 13, 2019 (153)
32	EVA_DECODE	ss3711837538	Jul 13, 2019 (153)
33	EVA_DECODE	ss3711837539	Jul 13, 2019 (153)
34	EVA_DECODE	ss3711837540	Jul 13, 2019 (153)
35	ACPOP	ss3731054787	Jul 13, 2019 (153)
36	ACPOP	ss3731054788	Jul 13, 2019 (153)
37	ACPOP	ss3731054789	Jul 13, 2019 (153)
38	PACBIO	ss3784681105	Jul 13, 2019 (153)
39	PACBIO	ss3790143900	Jul 13, 2019 (153)
40	PACBIO	ss3795019055	Jul 13, 2019 (153)
41	KHV_HUMAN_GENOMES	ss3804803880	Jul 13, 2019 (153)
42	KHV_HUMAN_GENOMES	ss3804803881	Jul 13, 2019 (153)
43	KHV_HUMAN_GENOMES	ss3804803882	Jul 13, 2019 (153)
44	EVA	ss3828485114	Apr 26, 2020 (154)
45	EVA	ss3843113991	Apr 26, 2020 (154)
46	KOGIC	ss3953924698	Apr 26, 2020 (154)
47	KOGIC	ss3953924699	Apr 26, 2020 (154)
48	KOGIC	ss3953924700	Apr 26, 2020 (154)
49	GNOMAD	ss4094244032	Apr 26, 2021 (155)
50	GNOMAD	ss4094244033	Apr 26, 2021 (155)
51	GNOMAD	ss4094244034	Apr 26, 2021 (155)
52	GNOMAD	ss4094244035	Apr 26, 2021 (155)
53	GNOMAD	ss4094244036	Apr 26, 2021 (155)
54	GNOMAD	ss4094244037	Apr 26, 2021 (155)
55	GNOMAD	ss4094244038	Apr 26, 2021 (155)
56	GNOMAD	ss4094244039	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5165157212	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5165157213	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5165157214	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5258803296	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5258803297	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5258803298	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5258803299	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5457629088	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5457629089	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5457629090	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5699066482	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5699066483	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5699066484	Oct 13, 2022 (156)
70	EVA	ss5843847464	Oct 13, 2022 (156)
71	EVA	ss5843847465	Oct 13, 2022 (156)
72	1000Genomes	NC_000004.11 - 39354648	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 802/3854) Row 11521871 (NC_000004.11:39354647::AC 1298/3854) Row 11521872 (NC_000004.11:39354668::CA 1476/3854)	-	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 802/3854) Row 11521871 (NC_000004.11:39354647::AC 1298/3854) Row 11521872 (NC_000004.11:39354668::CA 1476/3854)	-	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 802/3854) Row 11521871 (NC_000004.11:39354647::AC 1298/3854) Row 11521872 (NC_000004.11:39354668::CA 1476/3854)	-	Oct 12, 2018 (152)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146397591 (NC_000004.12:39353027::AC 45989/138918) Row 146397592 (NC_000004.12:39353027::ACAC 846/139000) Row 146397593 (NC_000004.12:39353027::ACACAC 78/139004)...	-	Apr 26, 2021 (155)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 10302699 (NC_000004.12:39353027:AC: 308/1832) Row 10302700 (NC_000004.12:39353029::AC 295/1832) Row 10302701 (NC_000004.12:39353029::ACAC 45/1832)	-	Apr 26, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 10302699 (NC_000004.12:39353027:AC: 308/1832) Row 10302700 (NC_000004.12:39353029::AC 295/1832) Row 10302701 (NC_000004.12:39353029::ACAC 45/1832)	-	Apr 26, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 10302699 (NC_000004.12:39353027:AC: 308/1832) Row 10302700 (NC_000004.12:39353029::AC 295/1832) Row 10302701 (NC_000004.12:39353029::ACAC 45/1832)	-	Apr 26, 2020 (154)
87	Northern Sweden Submission ignored due to conflicting rows: Row 4339652 (NC_000004.11:39354647:AC: 114/600) Row 4339653 (NC_000004.11:39354647::AC 224/600) Row 4339654 (NC_000004.11:39354647::ACAC 7/600)	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 4339652 (NC_000004.11:39354647:AC: 114/600) Row 4339653 (NC_000004.11:39354647::AC 224/600) Row 4339654 (NC_000004.11:39354647::ACAC 7/600)	-	Jul 13, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 4339652 (NC_000004.11:39354647:AC: 114/600) Row 4339653 (NC_000004.11:39354647::AC 224/600) Row 4339654 (NC_000004.11:39354647::ACAC 7/600)	-	Jul 13, 2019 (153)
90	8.3KJPN Submission ignored due to conflicting rows: Row 23126519 (NC_000004.11:39354647::AC 3626/16760) Row 23126520 (NC_000004.11:39354647:AC: 2768/16760) Row 23126521 (NC_000004.11:39354647::ACAC 306/16760)	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 23126519 (NC_000004.11:39354647::AC 3626/16760) Row 23126520 (NC_000004.11:39354647:AC: 2768/16760) Row 23126521 (NC_000004.11:39354647::ACAC 306/16760)	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 23126519 (NC_000004.11:39354647::AC 3626/16760) Row 23126520 (NC_000004.11:39354647:AC: 2768/16760) Row 23126521 (NC_000004.11:39354647::ACAC 306/16760)	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 32903586 (NC_000004.12:39353027::AC 6065/28258) Row 32903587 (NC_000004.12:39353027:AC: 4722/28258) Row 32903588 (NC_000004.12:39353027::ACAC 532/28258)	-	Oct 13, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 32903586 (NC_000004.12:39353027::AC 6065/28258) Row 32903587 (NC_000004.12:39353027:AC: 4722/28258) Row 32903588 (NC_000004.12:39353027::ACAC 532/28258)	-	Oct 13, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 32903586 (NC_000004.12:39353027::AC 6065/28258) Row 32903587 (NC_000004.12:39353027:AC: 4722/28258) Row 32903588 (NC_000004.12:39353027::ACAC 532/28258)	-	Oct 13, 2022 (156)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 819/3708) Row 11521871 (NC_000004.11:39354647::AC 1195/3708) Row 11521872 (NC_000004.11:39354668::CA 1353/3708)	-	Oct 12, 2018 (152)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 819/3708) Row 11521871 (NC_000004.11:39354647::AC 1195/3708) Row 11521872 (NC_000004.11:39354668::CA 1353/3708)	-	Oct 12, 2018 (152)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11521870 (NC_000004.11:39354647:AC: 819/3708) Row 11521871 (NC_000004.11:39354647::AC 1195/3708) Row 11521872 (NC_000004.11:39354668::CA 1353/3708)	-	Oct 12, 2018 (152)
99	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2529378 (NC_000004.11:39354647::ACAC 5/132) Row 2529379 (NC_000004.11:39354647:AC: 54/181) Row 2529380 (NC_000004.11:39354647::AC 28/155)	-	Jul 13, 2019 (153)
100	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2529378 (NC_000004.11:39354647::ACAC 5/132) Row 2529379 (NC_000004.11:39354647:AC: 54/181) Row 2529380 (NC_000004.11:39354647::AC 28/155)	-	Jul 13, 2019 (153)
101	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2529378 (NC_000004.11:39354647::ACAC 5/132) Row 2529379 (NC_000004.11:39354647:AC: 54/181) Row 2529380 (NC_000004.11:39354647::AC 28/155)	-	Jul 13, 2019 (153)
102	ALFA	NC_000004.12 - 39353028	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)
rs72297485	May 15, 2013 (138)
rs147549484	May 04, 2012 (137)
rs368827550	May 13, 2013 (138)
rs539307179	Apr 01, 2015 (144)
rs796905463	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4094244039	NC_000004.12:39353027:ACACACAC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACA	(self)
ss1801303930	NC_000004.11:39354647:ACACAC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACA	(self)
ss4094244038	NC_000004.12:39353027:ACACAC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACA	(self)
ss3711837540, ss4094244037	NC_000004.12:39353027:ACAC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACA	(self)
ss326509091, ss326539085, ss551353095, ss553117835	NC_000004.10:39031042:AC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
20678546, ss663507774, ss1372054897, ss1704122749, ss1704122769, ss1969714554, ss2994489840, ss3731054787, ss3828485114, ss5165157213, ss5843847465	NC_000004.11:39354647:AC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3064963279, ss3647701658, ss3804803882, ss3953924698, ss4094244036, ss5258803297, ss5457629088, ss5699066483	NC_000004.12:39353027:AC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3711837539	NC_000004.12:39353029:AC:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss95351692	NT_016297.16:6514028:CA:	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss326698713, ss551467952	NC_000004.10:39031042::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss288510239	NC_000004.10:39031063::CA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1536403365, ss1801303927, ss3731054788, ss3784681105, ss3790143900, ss3795019055, ss5165157212, ss5843847464	NC_000004.11:39354647::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1372054898, ss1710142112, ss1710142156	NC_000004.11:39354649::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1704122750, ss1704122773	NC_000004.11:39354668::CA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3064097202, ss3065944064, ss3843113991, ss4094244032, ss5258803296, ss5457629089, ss5699066482	NC_000004.12:39353027::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3804803881, ss3953924699	NC_000004.12:39353029::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3711837538	NC_000004.12:39353031::AC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss80377525, ss81067841	NT_016297.16:6514030::CA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3731054789, ss5165157214	NC_000004.11:39354647::ACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss1372054899	NC_000004.11:39354649::ACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4094244033, ss5258803298, ss5457629090, ss5699066484	NC_000004.12:39353027::ACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3804803880, ss3953924700	NC_000004.12:39353029::ACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3711837537	NC_000004.12:39353031::ACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4094244034, ss5258803299	NC_000004.12:39353027::ACACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3711837536	NC_000004.12:39353031::ACACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss4094244035	NC_000004.12:39353027::ACACACAC	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
13681409079	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000004.12:39353027:ACACACACACAC… NC_000004.12:39353027:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(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 rs59032726

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
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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

rs59032726