Name: rs3073060
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.

rs3073060

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:8911882-8911904 (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 / delCACA / delCA / dupCA…
del(CA)₄ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆
Variation Type: Indel Insertion and Deletion
Frequency: delCA=0.05635 (606/10754, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02676 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	10754	ACACACACACACACACACACACA=0.90599	ACACACACACACACA=0.00000, ACACACACACACACACACA=0.00009, ACACACACACACACACACACA=0.05635, ACACACACACACACACACACACACA=0.03673, ACACACACACACACACACACACACACA=0.00084, ACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACA=0.00000	0.897338	0.008405	0.094257	27
European	Sub	9210	ACACACACACACACACACACACA=0.8907	ACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0656, ACACACACACACACACACACACACA=0.0428, ACACACACACACACACACACACACACA=0.0010, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000	0.87911	0.009936	0.110953	20
African	Sub	992	ACACACACACACACACACACACA=1.000	ACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	42	ACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	950	ACACACACACACACACACACACA=1.000	ACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	12	ACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	8	ACACACACACACACACACACACA=1.0	ACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	ACACACACACACACACACACACA=1.0	ACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	60	ACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	220	ACACACACACACACACACACACA=1.000	ACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	36	ACACACACACACACACACACACA=1.00	ACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	224	ACACACACACACACACACACACA=0.982	ACACACACACACACA=0.000, ACACACACACACACACACA=0.004, ACACACACACACACACACACA=0.009, ACACACACACACACACACACACACA=0.004, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	0.981818	0.0	0.018182	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	10754	(AC)₁₁A=0.90599	del(CA)₄=0.00000, delCACA=0.00009, delCA=0.05635, dupCA=0.03673, dupCACA=0.00084, dup(CA)₃=0.00000, dup(CA)₄=0.00000, dup(CA)₅=0.00000, dup(CA)₆=0.00000
Allele Frequency Aggregator	European	Sub	9210	(AC)₁₁A=0.8907	del(CA)₄=0.0000, delCACA=0.0000, delCA=0.0656, dupCA=0.0428, dupCACA=0.0010, dup(CA)₃=0.0000, dup(CA)₄=0.0000, dup(CA)₅=0.0000, dup(CA)₆=0.0000
Allele Frequency Aggregator	African	Sub	992	(AC)₁₁A=1.000	del(CA)₄=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000
Allele Frequency Aggregator	Other	Sub	224	(AC)₁₁A=0.982	del(CA)₄=0.000, delCACA=0.004, delCA=0.009, dupCA=0.004, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	220	(AC)₁₁A=1.000	del(CA)₄=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(AC)₁₁A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	36	(AC)₁₁A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00
Allele Frequency Aggregator	Asian	Sub	12	(AC)₁₁A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00

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 10	NC_000010.11:g.8911883CA[7]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[9]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[10]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[12]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[13]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[14]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[15]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[16]
GRCh38.p14 chr 10	NC_000010.11:g.8911883CA[17]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[7]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[9]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[10]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[12]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[13]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[14]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[15]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[16]
GRCh37.p13 chr 10	NC_000010.10:g.8953846CA[17]

Gene: LINC02676, long intergenic non-protein coding RNA 2676 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02676 transcript	NR_131944.1: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)₁₁A=	del(CA)₄	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆
GRCh38.p14 chr 10	NC_000010.11:g.8911882_8911904=	NC_000010.11:g.8911883CA[7]	NC_000010.11:g.8911883CA[9]	NC_000010.11:g.8911883CA[10]	NC_000010.11:g.8911883CA[12]	NC_000010.11:g.8911883CA[13]	NC_000010.11:g.8911883CA[14]	NC_000010.11:g.8911883CA[15]	NC_000010.11:g.8911883CA[16]	NC_000010.11:g.8911883CA[17]
GRCh37.p13 chr 10	NC_000010.10:g.8953845_8953867=	NC_000010.10:g.8953846CA[7]	NC_000010.10:g.8953846CA[9]	NC_000010.10:g.8953846CA[10]	NC_000010.10:g.8953846CA[12]	NC_000010.10:g.8953846CA[13]	NC_000010.10:g.8953846CA[14]	NC_000010.10:g.8953846CA[15]	NC_000010.10:g.8953846CA[16]	NC_000010.10:g.8953846CA[17]

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#.

63 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4304453	Dec 03, 2013 (138)
2	ABI	ss39773580	Oct 12, 2018 (152)
3	BUSHMAN	ss193167977	Jul 04, 2010 (132)
4	GMI	ss288995883	May 04, 2012 (137)
5	1000GENOMES	ss327208084	May 09, 2011 (135)
6	1000GENOMES	ss327284552	Jan 10, 2018 (151)
7	1000GENOMES	ss327656294	May 09, 2011 (135)
8	LUNTER	ss551998201	Jan 10, 2018 (151)
9	LUNTER	ss552235947	Apr 25, 2013 (138)
10	LUNTER	ss553399675	Apr 25, 2013 (138)
11	SSMP	ss664010189	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666489523	Apr 25, 2013 (138)
13	DDI	ss1536641759	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1706631225	Jan 10, 2018 (151)
15	EVA_UK10K_TWINSUK	ss1706631473	Jan 10, 2018 (151)
16	EVA_UK10K_TWINSUK	ss1710452650	Oct 12, 2018 (152)
17	EVA_UK10K_ALSPAC	ss1710452796	Oct 12, 2018 (152)
18	HAMMER_LAB	ss1806249111	Sep 08, 2015 (146)
19	HAMMER_LAB	ss1806249112	Jan 10, 2018 (151)
20	GENOMED	ss1967055574	Jul 19, 2016 (147)
21	MCHAISSO	ss3064459561	Jan 10, 2018 (151)
22	EVA_DECODE	ss3689252286	Jul 13, 2019 (153)
23	EVA_DECODE	ss3689252287	Jul 13, 2019 (153)
24	EVA_DECODE	ss3689252288	Jul 13, 2019 (153)
25	EVA_DECODE	ss3689252289	Jul 13, 2019 (153)
26	ACPOP	ss3737048690	Jul 13, 2019 (153)
27	ACPOP	ss3737048691	Jul 13, 2019 (153)
28	ACPOP	ss3737048692	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3813089879	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3813089880	Jul 13, 2019 (153)
31	EVA	ss3831960234	Apr 26, 2020 (154)
32	EVA	ss3844977548	Apr 26, 2020 (154)
33	GNOMAD	ss4212668476	Apr 26, 2021 (155)
34	GNOMAD	ss4212668477	Apr 26, 2021 (155)
35	GNOMAD	ss4212668478	Apr 26, 2021 (155)
36	GNOMAD	ss4212668479	Apr 26, 2021 (155)
37	GNOMAD	ss4212668480	Apr 26, 2021 (155)
38	GNOMAD	ss4212668481	Apr 26, 2021 (155)
39	GNOMAD	ss4212668484	Apr 26, 2021 (155)
40	GNOMAD	ss4212668485	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5196194341	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5196194342	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5196194343	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5196194344	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5196194345	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5282865168	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5282865169	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5282865170	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5282865171	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5478649353	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5478649354	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5478649355	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5478649356	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5478649357	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5478649358	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5741021846	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5741021847	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5741021848	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5741021849	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5741021850	Oct 16, 2022 (156)
61	EVA	ss5823955029	Oct 16, 2022 (156)
62	EVA	ss5823955030	Oct 16, 2022 (156)
63	EVA	ss5849431085	Oct 16, 2022 (156)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26982803 (NC_000010.10:8953844:AC: 645/3854) Row 26982804 (NC_000010.10:8953844::AC 306/3854)	-	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26982803 (NC_000010.10:8953844:AC: 645/3854) Row 26982804 (NC_000010.10:8953844::AC 306/3854)	-	Oct 12, 2018 (152)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343005101 (NC_000010.11:8911881::AC 23928/138126) Row 343005102 (NC_000010.11:8911881::ACAC 2185/138186) Row 343005103 (NC_000010.11:8911881::ACACAC 328/138196)...	-	Apr 26, 2021 (155)
74	Northern Sweden Submission ignored due to conflicting rows: Row 10333555 (NC_000010.10:8953844:AC: 111/600) Row 10333556 (NC_000010.10:8953844::AC 31/600) Row 10333557 (NC_000010.10:8953844::ACAC 2/600)	-	Jul 13, 2019 (153)
75	Northern Sweden Submission ignored due to conflicting rows: Row 10333555 (NC_000010.10:8953844:AC: 111/600) Row 10333556 (NC_000010.10:8953844::AC 31/600) Row 10333557 (NC_000010.10:8953844::ACAC 2/600)	-	Jul 13, 2019 (153)
76	Northern Sweden Submission ignored due to conflicting rows: Row 10333555 (NC_000010.10:8953844:AC: 111/600) Row 10333556 (NC_000010.10:8953844::AC 31/600) Row 10333557 (NC_000010.10:8953844::ACAC 2/600)	-	Jul 13, 2019 (153)
77	8.3KJPN Submission ignored due to conflicting rows: Row 54163648 (NC_000010.10:8953844::AC 9070/16760) Row 54163649 (NC_000010.10:8953844:AC: 765/16760) Row 54163650 (NC_000010.10:8953844::ACAC 367/16760)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 54163648 (NC_000010.10:8953844::AC 9070/16760) Row 54163649 (NC_000010.10:8953844:AC: 765/16760) Row 54163650 (NC_000010.10:8953844::ACAC 367/16760)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 54163648 (NC_000010.10:8953844::AC 9070/16760) Row 54163649 (NC_000010.10:8953844:AC: 765/16760) Row 54163650 (NC_000010.10:8953844::ACAC 367/16760)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 54163648 (NC_000010.10:8953844::AC 9070/16760) Row 54163649 (NC_000010.10:8953844:AC: 765/16760) Row 54163650 (NC_000010.10:8953844::ACAC 367/16760)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 54163648 (NC_000010.10:8953844::AC 9070/16760) Row 54163649 (NC_000010.10:8953844:AC: 765/16760) Row 54163650 (NC_000010.10:8953844::ACAC 367/16760)...	-	Apr 26, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 74858950 (NC_000010.11:8911881:AC: 1269/28258) Row 74858951 (NC_000010.11:8911881::AC 15379/28258) Row 74858952 (NC_000010.11:8911881::ACAC 641/28258)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 74858950 (NC_000010.11:8911881:AC: 1269/28258) Row 74858951 (NC_000010.11:8911881::AC 15379/28258) Row 74858952 (NC_000010.11:8911881::ACAC 641/28258)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 74858950 (NC_000010.11:8911881:AC: 1269/28258) Row 74858951 (NC_000010.11:8911881::AC 15379/28258) Row 74858952 (NC_000010.11:8911881::ACAC 641/28258)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 74858950 (NC_000010.11:8911881:AC: 1269/28258) Row 74858951 (NC_000010.11:8911881::AC 15379/28258) Row 74858952 (NC_000010.11:8911881::ACAC 641/28258)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 74858950 (NC_000010.11:8911881:AC: 1269/28258) Row 74858951 (NC_000010.11:8911881::AC 15379/28258) Row 74858952 (NC_000010.11:8911881::ACAC 641/28258)...	-	Oct 16, 2022 (156)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26982803 (NC_000010.10:8953844:AC: 649/3708) Row 26982804 (NC_000010.10:8953844::AC 278/3708)	-	Oct 12, 2018 (152)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26982803 (NC_000010.10:8953844:AC: 649/3708) Row 26982804 (NC_000010.10:8953844::AC 278/3708)	-	Oct 12, 2018 (152)
89	ALFA	NC_000010.11 - 8911882	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)
rs36114816	May 15, 2013 (138)
rs372287352	May 13, 2013 (138)
rs796861787	Nov 08, 2017 (151)
rs143639128	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACA	(self)
ss3689252289, ss4212668485	NC_000010.11:8911881:ACAC:	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss327284552, ss551998201	NC_000010.9:8993850:AC:	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss1706631225, ss1706631473, ss1806249112, ss3737048690, ss5196194342, ss5823955030	NC_000010.10:8953844:AC:	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3064459561, ss4212668484, ss5282865169, ss5478649354, ss5741021846	NC_000010.11:8911881:AC:	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3689252288	NC_000010.11:8911883:AC:	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss327208084, ss327656294, ss552235947, ss553399675	NC_000010.9:8993850::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss288995883	NC_000010.9:8993873::CA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss664010189, ss666489523, ss1536641759, ss1806249111, ss1967055574, ss3737048691, ss3831960234, ss5196194341, ss5823955029	NC_000010.10:8953844::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss1710452650, ss1710452796	NC_000010.10:8953846::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3813089879, ss3844977548, ss4212668476, ss5282865168, ss5478649353, ss5741021847, ss5849431085	NC_000010.11:8911881::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3689252287	NC_000010.11:8911885::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss39773580	NT_008705.16:8893866::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4304453	NT_008705.16:8893867::CA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss193167977	NT_008705.17:8901881::AC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3737048692, ss5196194343	NC_000010.10:8953844::ACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3813089880, ss4212668477, ss5282865170, ss5478649356, ss5741021848	NC_000010.11:8911881::ACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3689252286	NC_000010.11:8911885::ACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss5196194344	NC_000010.10:8953844::ACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss4212668478, ss5478649355, ss5741021849	NC_000010.11:8911881::ACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss5196194345	NC_000010.10:8953844::ACACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4212668479, ss5478649357, ss5741021850	NC_000010.11:8911881::ACACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4212668480, ss5282865171, ss5478649358	NC_000010.11:8911881::ACACACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss4212668481	NC_000010.11:8911881::ACACACACACAC	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
11472000059	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	NC_000010.11:8911881:ACACACACACACA… NC_000010.11:8911881:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(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 rs3073060

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs3073060