Name: rs370152468
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.

rs370152468

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:116650914-116650934 (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=0.01454 (202/13896, ALFA)
dupCA=0.1014 (508/5008, 1000G)
dupCA=0.019 (4/216, Vietnamese) (+ 1 more)
dupCA=0.03 (1/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZUP1 : 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	13896	ACACACACACACACACACACA=0.98381	ACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00151, ACACACACACACACACACACACA=0.01454, ACACACACACACACACACACACACA=0.00014, ACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACA=0.00000	0.971408	0.000433	0.028159	1
European	Sub	10912	ACACACACACACACACACACA=0.97938	ACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00192, ACACACACACACACACACACACA=0.01851, ACACACACACACACACACACACACA=0.00018, ACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACA=0.00000	0.963556	0.000552	0.035892	0
African	Sub	1930	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	78	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1852	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	112	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	392	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	384	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A

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	13896	(AC)₁₀A=0.98381	del(CA)₄=0.00000, delCACA=0.00000, delCA=0.00151, dupCA=0.01454, dupCACA=0.00014, dup(CA)₃=0.00000, dup(CA)₄=0.00000
Allele Frequency Aggregator	European	Sub	10912	(AC)₁₀A=0.97938	del(CA)₄=0.00000, delCACA=0.00000, delCA=0.00192, dupCA=0.01851, dupCACA=0.00018, dup(CA)₃=0.00000, dup(CA)₄=0.00000
Allele Frequency Aggregator	African	Sub	1930	(AC)₁₀A=1.0000	del(CA)₄=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	392	(AC)₁₀A=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
Allele Frequency Aggregator	Other	Sub	384	(AC)₁₀A=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
Allele Frequency Aggregator	Latin American 1	Sub	112	(AC)₁₀A=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
Allele Frequency Aggregator	Asian	Sub	94	(AC)₁₀A=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
Allele Frequency Aggregator	South Asian	Sub	72	(AC)₁₀A=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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCA=0.1014, dupCACA=0.0036
1000Genomes	African	Sub	1322	- No frequency provided	dupCA=0.1551, dupCACA=0.0121
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCA=0.0228, dupCACA=0.0000
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCA=0.0656, dupCACA=0.0000
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCA=0.079, dupCACA=0.001
1000Genomes	American	Sub	694	- No frequency provided	dupCA=0.197, dupCACA=0.001
A Vietnamese Genetic Variation Database	Global	Study-wide	216	- No frequency provided	dupCA=0.019
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupCA=0.03

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 6	NC_000006.12:g.116650915CA[6]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[7]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[8]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[9]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[11]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[12]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[13]
GRCh38.p14 chr 6	NC_000006.12:g.116650915CA[14]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[6]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[7]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[8]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[9]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[11]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[12]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[13]
GRCh37.p13 chr 6	NC_000006.11:g.116972078CA[14]

Gene: ZUP1, zinc finger containing ubiquitin peptidase 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZUP1 transcript variant 2	NM_001361189.2:c.1316+639… NM_001361189.2:c.1316+639GT[6]	N/A	Intron Variant
ZUP1 transcript variant 3	NM_001361190.2:c.812+639G… NM_001361190.2:c.812+639GT[6]	N/A	Intron Variant
ZUP1 transcript variant 6	NM_001361191.2:c.728+639G… NM_001361191.2:c.728+639GT[6]	N/A	Intron Variant
ZUP1 transcript variant 1	NM_145062.3:c.1316+639GT[… NM_145062.3:c.1316+639GT[6]	N/A	Intron Variant
ZUP1 transcript variant 4	NR_154586.2:n.	N/A	Intron Variant
ZUP1 transcript variant 5	NR_154587.2:n.	N/A	Intron Variant
ZUP1 transcript variant 7	NR_154588.2:n.	N/A	Intron Variant
ZUP1 transcript variant 8	NR_154589.2: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 6	NC_000006.12:g.116650914_116650934=	NC_000006.12:g.116650915CA[6]	NC_000006.12:g.116650915CA[7]	NC_000006.12:g.116650915CA[8]	NC_000006.12:g.116650915CA[9]	NC_000006.12:g.116650915CA[11]	NC_000006.12:g.116650915CA[12]	NC_000006.12:g.116650915CA[13]	NC_000006.12:g.116650915CA[14]
GRCh37.p13 chr 6	NC_000006.11:g.116972077_116972097=	NC_000006.11:g.116972078CA[6]	NC_000006.11:g.116972078CA[7]	NC_000006.11:g.116972078CA[8]	NC_000006.11:g.116972078CA[9]	NC_000006.11:g.116972078CA[11]	NC_000006.11:g.116972078CA[12]	NC_000006.11:g.116972078CA[13]	NC_000006.11:g.116972078CA[14]
ZUP1 transcript variant 2	NM_001361189.2:c.1316+658=	NM_001361189.2:c.1316+639GT[6]	NM_001361189.2:c.1316+639GT[7]	NM_001361189.2:c.1316+639GT[8]	NM_001361189.2:c.1316+639GT[9]	NM_001361189.2:c.1316+639GT[11]	NM_001361189.2:c.1316+639GT[12]	NM_001361189.2:c.1316+639GT[13]	NM_001361189.2:c.1316+639GT[14]
ZUP1 transcript variant 3	NM_001361190.2:c.812+658=	NM_001361190.2:c.812+639GT[6]	NM_001361190.2:c.812+639GT[7]	NM_001361190.2:c.812+639GT[8]	NM_001361190.2:c.812+639GT[9]	NM_001361190.2:c.812+639GT[11]	NM_001361190.2:c.812+639GT[12]	NM_001361190.2:c.812+639GT[13]	NM_001361190.2:c.812+639GT[14]
ZUP1 transcript variant 6	NM_001361191.2:c.728+658=	NM_001361191.2:c.728+639GT[6]	NM_001361191.2:c.728+639GT[7]	NM_001361191.2:c.728+639GT[8]	NM_001361191.2:c.728+639GT[9]	NM_001361191.2:c.728+639GT[11]	NM_001361191.2:c.728+639GT[12]	NM_001361191.2:c.728+639GT[13]	NM_001361191.2:c.728+639GT[14]
ZUP1 transcript variant 1	NM_145062.2:c.1316+658=	NM_145062.2:c.1316+639GT[6]	NM_145062.2:c.1316+639GT[7]	NM_145062.2:c.1316+639GT[8]	NM_145062.2:c.1316+639GT[9]	NM_145062.2:c.1316+639GT[11]	NM_145062.2:c.1316+639GT[12]	NM_145062.2:c.1316+639GT[13]	NM_145062.2:c.1316+639GT[14]
ZUP1 transcript variant 1	NM_145062.3:c.1316+658=	NM_145062.3:c.1316+639GT[6]	NM_145062.3:c.1316+639GT[7]	NM_145062.3:c.1316+639GT[8]	NM_145062.3:c.1316+639GT[9]	NM_145062.3:c.1316+639GT[11]	NM_145062.3:c.1316+639GT[12]	NM_145062.3:c.1316+639GT[13]	NM_145062.3:c.1316+639GT[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#.

52 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss326902011	Oct 12, 2018 (152)
2	1000GENOMES	ss327162090	Oct 12, 2018 (152)
3	LUNTER	ss551657050	Oct 12, 2018 (152)
4	LUNTER	ss551849213	Apr 25, 2013 (138)
5	SSMP	ss663644696	Apr 01, 2015 (144)
6	SSIP	ss947178998	Aug 21, 2014 (142)
7	1000GENOMES	ss1376052886	Aug 21, 2014 (142)
8	1000GENOMES	ss1376052889	Aug 21, 2014 (142)
9	DDI	ss1536519828	Apr 01, 2015 (144)
10	EVA_GENOME_DK	ss1576841982	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1705333068	Oct 12, 2018 (152)
12	EVA_UK10K_TWINSUK	ss1705333443	Oct 12, 2018 (152)
13	EVA_UK10K_ALSPAC	ss1710289963	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1710289981	Apr 01, 2015 (144)
15	JJLAB	ss2030790851	Sep 14, 2016 (149)
16	SWEGEN	ss2999814650	Nov 17, 2017 (151)
17	MCHAISSO	ss3066103007	Nov 08, 2017 (151)
18	EVA_DECODE	ss3718110697	Jul 13, 2019 (153)
19	EVA_DECODE	ss3718110698	Jul 13, 2019 (153)
20	EVA_DECODE	ss3718110699	Jul 13, 2019 (153)
21	EVA_DECODE	ss3718110700	Jul 13, 2019 (153)
22	ACPOP	ss3733907295	Jul 13, 2019 (153)
23	ACPOP	ss3733907296	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3808720380	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3808720381	Jul 13, 2019 (153)
26	KOGIC	ss3959920381	Apr 26, 2020 (154)
27	KOGIC	ss3959920382	Apr 26, 2020 (154)
28	KOGIC	ss3959920383	Apr 26, 2020 (154)
29	GNOMAD	ss4149905757	Apr 26, 2021 (155)
30	GNOMAD	ss4149905758	Apr 26, 2021 (155)
31	GNOMAD	ss4149905759	Apr 26, 2021 (155)
32	GNOMAD	ss4149905760	Apr 26, 2021 (155)
33	GNOMAD	ss4149905761	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5179546843	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5179546844	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5179546845	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5179546846	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5270049881	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5270049882	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5270049883	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5270049884	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5467519945	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5467519946	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5467519947	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5467519948	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5718326635	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5718326636	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5718326637	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5718326638	Oct 13, 2022 (156)
50	YY_MCH	ss5807883208	Oct 13, 2022 (156)
51	EVA	ss5842872079	Oct 13, 2022 (156)
52	EVA	ss5842872080	Oct 13, 2022 (156)
53	1000Genomes	NC_000006.11 - 116972077	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 18827725 (NC_000006.11:116972076::AC 328/3854) Row 18827726 (NC_000006.11:116972076:AC: 166/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 18827725 (NC_000006.11:116972076::AC 328/3854) Row 18827726 (NC_000006.11:116972076:AC: 166/3854)	-	Oct 12, 2018 (152)
56	The Danish reference pan genome	NC_000006.11 - 116972077	Apr 26, 2020 (154)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238593512 (NC_000006.12:116650913::AC 13642/137764) Row 238593513 (NC_000006.12:116650913::ACAC 783/137828) Row 238593514 (NC_000006.12:116650913::ACACAC 15/137834)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238593512 (NC_000006.12:116650913::AC 13642/137764) Row 238593513 (NC_000006.12:116650913::ACAC 783/137828) Row 238593514 (NC_000006.12:116650913::ACACAC 15/137834)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238593512 (NC_000006.12:116650913::AC 13642/137764) Row 238593513 (NC_000006.12:116650913::ACAC 783/137828) Row 238593514 (NC_000006.12:116650913::ACACAC 15/137834)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238593512 (NC_000006.12:116650913::AC 13642/137764) Row 238593513 (NC_000006.12:116650913::ACAC 783/137828) Row 238593514 (NC_000006.12:116650913::ACACAC 15/137834)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 238593512 (NC_000006.12:116650913::AC 13642/137764) Row 238593513 (NC_000006.12:116650913::ACAC 783/137828) Row 238593514 (NC_000006.12:116650913::ACACAC 15/137834)...	-	Apr 26, 2021 (155)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 16298382 (NC_000006.12:116650913:AC: 21/1832) Row 16298383 (NC_000006.12:116650915::AC 99/1832) Row 16298384 (NC_000006.12:116650915::ACAC 2/1832)	-	Apr 26, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 16298382 (NC_000006.12:116650913:AC: 21/1832) Row 16298383 (NC_000006.12:116650915::AC 99/1832) Row 16298384 (NC_000006.12:116650915::ACAC 2/1832)	-	Apr 26, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 16298382 (NC_000006.12:116650913:AC: 21/1832) Row 16298383 (NC_000006.12:116650915::AC 99/1832) Row 16298384 (NC_000006.12:116650915::ACAC 2/1832)	-	Apr 26, 2020 (154)
65	Northern Sweden Submission ignored due to conflicting rows: Row 7192160 (NC_000006.11:116972076::AC 54/600) Row 7192161 (NC_000006.11:116972076:AC: 11/600)	-	Jul 13, 2019 (153)
66	Northern Sweden Submission ignored due to conflicting rows: Row 7192160 (NC_000006.11:116972076::AC 54/600) Row 7192161 (NC_000006.11:116972076:AC: 11/600)	-	Jul 13, 2019 (153)
67	8.3KJPN Submission ignored due to conflicting rows: Row 37516150 (NC_000006.11:116972076::AC 1084/16760) Row 37516151 (NC_000006.11:116972076:AC: 16/16760) Row 37516152 (NC_000006.11:116972076::ACAC 7/16760)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 37516150 (NC_000006.11:116972076::AC 1084/16760) Row 37516151 (NC_000006.11:116972076:AC: 16/16760) Row 37516152 (NC_000006.11:116972076::ACAC 7/16760)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 37516150 (NC_000006.11:116972076::AC 1084/16760) Row 37516151 (NC_000006.11:116972076:AC: 16/16760) Row 37516152 (NC_000006.11:116972076::ACAC 7/16760)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 37516150 (NC_000006.11:116972076::AC 1084/16760) Row 37516151 (NC_000006.11:116972076:AC: 16/16760) Row 37516152 (NC_000006.11:116972076::ACAC 7/16760)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 52163739 (NC_000006.12:116650913::AC 1837/28258) Row 52163740 (NC_000006.12:116650913:AC: 9/28258) Row 52163741 (NC_000006.12:116650913::ACAC 11/28258)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 52163739 (NC_000006.12:116650913::AC 1837/28258) Row 52163740 (NC_000006.12:116650913:AC: 9/28258) Row 52163741 (NC_000006.12:116650913::ACAC 11/28258)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 52163739 (NC_000006.12:116650913::AC 1837/28258) Row 52163740 (NC_000006.12:116650913:AC: 9/28258) Row 52163741 (NC_000006.12:116650913::ACAC 11/28258)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 52163739 (NC_000006.12:116650913::AC 1837/28258) Row 52163740 (NC_000006.12:116650913:AC: 9/28258) Row 52163741 (NC_000006.12:116650913::ACAC 11/28258)...	-	Oct 13, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 18827725 (NC_000006.11:116972076::AC 328/3708) Row 18827726 (NC_000006.11:116972076:AC: 183/3708)	-	Oct 12, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 18827725 (NC_000006.11:116972076::AC 328/3708) Row 18827726 (NC_000006.11:116972076:AC: 183/3708)	-	Oct 12, 2018 (152)
77	A Vietnamese Genetic Variation Database	NC_000006.11 - 116972077	Jul 13, 2019 (153)
78	ALFA	NC_000006.12 - 116650914	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4149905761	NC_000006.12:116650913:ACACACAC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACA	(self)
ss5179546846	NC_000006.11:116972076:ACACAC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACA	(self)
ss5718326638	NC_000006.12:116650913:ACACAC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACA
ss3718110700	NC_000006.12:116650913:ACAC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACA	(self)
ss326902011, ss551657050	NC_000006.10:117078769:AC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss1705333068, ss1705333443, ss2999814650, ss3733907296, ss5179546844, ss5842872079	NC_000006.11:116972076:AC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3959920381, ss4149905760, ss5270049884, ss5467519946, ss5718326636	NC_000006.12:116650913:AC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3718110699	NC_000006.12:116650915:AC:	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss327162090, ss551849213	NC_000006.10:117078769::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
33785655, 1103232, 4188137, ss663644696, ss947178998, ss1376052886, ss1536519828, ss1576841982, ss2030790851, ss3733907295, ss5179546843, ss5842872080	NC_000006.11:116972076::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1710289963, ss1710289981	NC_000006.11:116972078::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3066103007, ss3808720380, ss4149905757, ss5270049881, ss5467519945, ss5718326635, ss5807883208	NC_000006.12:116650913::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3808720381, ss3959920382	NC_000006.12:116650915::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3718110698	NC_000006.12:116650917::AC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
33785655, ss1376052889, ss5179546845	NC_000006.11:116972076::ACAC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4149905758, ss5270049882, ss5467519947, ss5718326637	NC_000006.12:116650913::ACAC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3959920383	NC_000006.12:116650915::ACAC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3718110697	NC_000006.12:116650917::ACAC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4149905759, ss5270049883, ss5467519948	NC_000006.12:116650913::ACACAC	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
7732781343	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000006.12:116650913:ACACACACACA… NC_000006.12:116650913: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 rs370152468

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

rs370152468