Name: rs75673310
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.

rs75673310

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:22489679-22489689 (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: delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.160928 (42596/264690, TOPMED)
dupA=0.24230 (3580/14775, ALFA)
(A)₁₁=0.3072 (1492/4856, 1000G) (+ 4 more)
(A)₁₁=0.1859 (806/4336, Estonian)
(A)₁₁=0.142 (142/998, GoNL)
(A)₁₁=0.133 (80/600, NorthernSweden)
(A)₁₁=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF280B : 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	14775	AAAAAAAAAAA=0.75635	AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.24230, AAAAAAAAAAAAA=0.00135	0.716465	0.196105	0.08743	32
European	Sub	11931	AAAAAAAAAAA=0.69885	AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.29947, AAAAAAAAAAAAA=0.00168	0.649046	0.242695	0.108259	32
African	Sub	1848	AAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	78	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1770	AAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	50	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	AAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	106	AAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	446	AAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	52	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	342	AAAAAAAAAAA=0.980	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.020, AAAAAAAAAAAAA=0.000	0.976608	0.017544	0.005848	32

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₁₁=0.839072	delA=0.160928
Allele Frequency Aggregator	Total	Global	14775	(A)₁₁=0.75635	delAA=0.00000, delA=0.00000, dupA=0.24230, dupAA=0.00135
Allele Frequency Aggregator	European	Sub	11931	(A)₁₁=0.69885	delAA=0.00000, delA=0.00000, dupA=0.29947, dupAA=0.00168
Allele Frequency Aggregator	African	Sub	1848	(A)₁₁=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	446	(A)₁₁=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	342	(A)₁₁=0.980	delAA=0.000, delA=0.000, dupA=0.020, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	106	(A)₁₁=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	52	(A)₁₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	50	(A)₁₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	4856	- No frequency provided	dupA=0.6928
1000Genomes	African	Sub	1209	- No frequency provided	dupA=0.6849
1000Genomes	East Asian	Sub	1007	- No frequency provided	dupA=0.6584
1000Genomes	Europe	Sub	996	- No frequency provided	dupA=0.774
1000Genomes	South Asian	Sub	955	- No frequency provided	dupA=0.597
1000Genomes	American	Sub	689	- No frequency provided	dupA=0.772
Genetic variation in the Estonian population	Estonian	Study-wide	4336	- No frequency provided	dupA=0.8141
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupA=0.858
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupA=0.867
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.85

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 22	NC_000022.11:g.22489688_22489689del
GRCh38.p14 chr 22	NC_000022.11:g.22489689del
GRCh38.p14 chr 22	NC_000022.11:g.22489689dup
GRCh38.p14 chr 22	NC_000022.11:g.22489688_22489689dup
GRCh37.p13 chr 22	NC_000022.10:g.22844013dup
GRCh37.p13 chr 22	NC_000022.10:g.22844013del
GRCh37.p13 chr 22	NC_000022.10:g.22844012_22844013dup
GRCh37.p13 chr 22	NC_000022.10:g.22844011_22844013dup
IGL genomic region	NG_000002.1:g.468001dup
IGL genomic region	NG_000002.1:g.468001del
IGL genomic region	NG_000002.1:g.468000_468001dup
IGL genomic region	NG_000002.1:g.467999_468001dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG3	NT_187629.1:g.125345_125346del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG3	NT_187629.1:g.125346del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG3	NT_187629.1:g.125346dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG3	NT_187629.1:g.125345_125346dup

Gene: ZNF280B, zinc finger protein 280B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF280B transcript variant 1	NM_080764.4:c.-68-214_-68… NM_080764.4:c.-68-214_-68-213del	N/A	Intron Variant
ZNF280B transcript variant 2	NR_130642.2:n.	N/A	Intron Variant
ZNF280B transcript variant 3	NR_130643.2:n.	N/A	Intron Variant
ZNF280B transcript variant X3	XM_011529897.3:c.-68-214_… XM_011529897.3:c.-68-214_-68-213del	N/A	Intron Variant
ZNF280B transcript variant X1	XM_047441143.1:c.-68-214_… XM_047441143.1:c.-68-214_-68-213del	N/A	Intron Variant
ZNF280B transcript variant X2	XM_047441144.1:c.-68-214_… XM_047441144.1:c.-68-214_-68-213del	N/A	Intron Variant
ZNF280B transcript variant X4	XM_047441145.1:c.-68-214_… XM_047441145.1:c.-68-214_-68-213del	N/A	Intron Variant
ZNF280B transcript variant X5	XM_047441146.1:c.-68-214_… XM_047441146.1:c.-68-214_-68-213del	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	(A)₁₁=	delAA	delA	dupA	dupAA
GRCh38.p14 chr 22	NC_000022.11:g.22489679_22489689=	NC_000022.11:g.22489688_22489689del	NC_000022.11:g.22489689del	NC_000022.11:g.22489689dup	NC_000022.11:g.22489688_22489689dup
GRCh37.p13 chr 22	NC_000022.10:g.22844013dup	NC_000022.10:g.22844013del	NC_000022.10:g.22844004_22844013=	NC_000022.10:g.22844012_22844013dup	NC_000022.10:g.22844011_22844013dup
IGL genomic region	NG_000002.1:g.468001dup	NG_000002.1:g.468001del	NG_000002.1:g.467992_468001=	NG_000002.1:g.468000_468001dup	NG_000002.1:g.467999_468001dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG3	NT_187629.1:g.125336_125346=	NT_187629.1:g.125345_125346del	NT_187629.1:g.125346del	NT_187629.1:g.125346dup	NT_187629.1:g.125345_125346dup
ZNF280B transcript	NM_080764.2:c.-68-213dup	NM_080764.2:c.-68-213del	NM_080764.2:c.-68-213=	NM_080764.2:c.-68-214_-68-213dup	NM_080764.2:c.-68-215_-68-213dup
ZNF280B transcript variant 1	NM_080764.4:c.-68-213=	NM_080764.4:c.-68-214_-68-213del	NM_080764.4:c.-68-213del	NM_080764.4:c.-68-213dup	NM_080764.4:c.-68-214_-68-213dup
ZNF280B transcript variant X1	XM_005261338.1:c.-68-213dup	XM_005261338.1:c.-68-213del	XM_005261338.1:c.-68-213=	XM_005261338.1:c.-68-214_-68-213dup	XM_005261338.1:c.-68-215_-68-213dup
ZNF280B transcript variant X3	XM_011529897.3:c.-68-213=	XM_011529897.3:c.-68-214_-68-213del	XM_011529897.3:c.-68-213del	XM_011529897.3:c.-68-213dup	XM_011529897.3:c.-68-214_-68-213dup
ZNF280B transcript variant X1	XM_047441143.1:c.-68-213=	XM_047441143.1:c.-68-214_-68-213del	XM_047441143.1:c.-68-213del	XM_047441143.1:c.-68-213dup	XM_047441143.1:c.-68-214_-68-213dup
ZNF280B transcript variant X2	XM_047441144.1:c.-68-213=	XM_047441144.1:c.-68-214_-68-213del	XM_047441144.1:c.-68-213del	XM_047441144.1:c.-68-213dup	XM_047441144.1:c.-68-214_-68-213dup
ZNF280B transcript variant X4	XM_047441145.1:c.-68-213=	XM_047441145.1:c.-68-214_-68-213del	XM_047441145.1:c.-68-213del	XM_047441145.1:c.-68-213dup	XM_047441145.1:c.-68-214_-68-213dup
ZNF280B transcript variant X5	XM_047441146.1:c.-68-213=	XM_047441146.1:c.-68-214_-68-213del	XM_047441146.1:c.-68-213del	XM_047441146.1:c.-68-213dup	XM_047441146.1:c.-68-214_-68-213dup

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#.

55 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95754589	Apr 25, 2013 (138)
2	BGI	ss104736492	Dec 01, 2009 (131)
3	BUSHMAN	ss193641154	Jul 04, 2010 (132)
4	BL	ss256190889	May 09, 2011 (135)
5	GMI	ss288553217	Apr 25, 2013 (138)
6	GMI	ss289442238	May 31, 2013 (142)
7	PJP	ss295072900	May 31, 2013 (138)
8	PJP	ss295072901	May 31, 2013 (138)
9	1000GENOMES	ss327999776	May 09, 2011 (135)
10	1000GENOMES	ss328101091	May 09, 2011 (135)
11	1000GENOMES	ss328322744	May 09, 2011 (135)
12	LUNTER	ss552710025	Apr 25, 2013 (138)
13	LUNTER	ss553133536	Apr 25, 2013 (138)
14	LUNTER	ss553699956	Apr 25, 2013 (138)
15	SSMP	ss664517966	Apr 09, 2015 (144)
16	BILGI_BIOE	ss666767244	Apr 25, 2013 (138)
17	EVA-GONL	ss995240904	Apr 09, 2015 (144)
18	1000GENOMES	ss1378916043	Aug 28, 2014 (142)
19	DDI	ss1536927274	Apr 09, 2015 (144)
20	EVA_GENOME_DK	ss1575812672	Apr 09, 2015 (144)
21	EVA_DECODE	ss1699309524	Apr 09, 2015 (144)
22	HAMMER_LAB	ss1809741819	Sep 11, 2015 (146)
23	SWEGEN	ss3019130952	Oct 12, 2018 (152)
24	BEROUKHIMLAB	ss3644458344	Oct 12, 2018 (152)
25	BIOINF_KMB_FNS_UNIBA	ss3645678339	Oct 12, 2018 (152)
26	EGCUT_WGS	ss3685643625	Jul 13, 2019 (153)
27	EVA_DECODE	ss3707989613	Jul 13, 2019 (153)
28	EVA_DECODE	ss3707989614	Jul 13, 2019 (153)
29	ACPOP	ss3743840135	Jul 13, 2019 (153)
30	PACBIO	ss3788799121	Jul 13, 2019 (153)
31	PACBIO	ss3793669521	Jul 13, 2019 (153)
32	PACBIO	ss3798555870	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3822420459	Jul 13, 2019 (153)
34	EVA	ss3835936694	Apr 27, 2020 (154)
35	EVA	ss3841597206	Apr 27, 2020 (154)
36	VINODS	ss4034753028	Apr 27, 2021 (155)
37	GNOMAD	ss4362862870	Apr 27, 2021 (155)
38	GNOMAD	ss4362862871	Apr 27, 2021 (155)
39	GNOMAD	ss4362862872	Apr 27, 2021 (155)
40	GNOMAD	ss4362862873	Apr 27, 2021 (155)
41	TOPMED	ss5105693097	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5232149664	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5232149665	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5232149666	Apr 27, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5310728540	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5310728541	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5310728542	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5502619811	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5502619812	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5793122330	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5793122331	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5793122333	Oct 16, 2022 (156)
53	EVA	ss5821927585	Oct 16, 2022 (156)
54	EVA	ss5853353629	Oct 16, 2022 (156)
55	EVA	ss5981126135	Oct 16, 2022 (156)
56	1000Genomes	NC_000022.10 - 22844004	Oct 12, 2018 (152)
57	Genetic variation in the Estonian population	NC_000022.10 - 22844004	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000022.10 - 22844004	Apr 27, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 567057483 (NC_000022.11:22489678::A 185/134128) Row 567057484 (NC_000022.11:22489678::AA 1/134180) Row 567057485 (NC_000022.11:22489678:A: 21564/134058)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 567057483 (NC_000022.11:22489678::A 185/134128) Row 567057484 (NC_000022.11:22489678::AA 1/134180) Row 567057485 (NC_000022.11:22489678:A: 21564/134058)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 567057483 (NC_000022.11:22489678::A 185/134128) Row 567057484 (NC_000022.11:22489678::AA 1/134180) Row 567057485 (NC_000022.11:22489678:A: 21564/134058)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 567057483 (NC_000022.11:22489678::A 185/134128) Row 567057484 (NC_000022.11:22489678::AA 1/134180) Row 567057485 (NC_000022.11:22489678:A: 21564/134058)...	-	Apr 27, 2021 (155)
63	Genome of the Netherlands Release 5	NC_000022.10 - 22844004	Apr 27, 2020 (154)
64	Northern Sweden	NC_000022.10 - 22844004	Jul 13, 2019 (153)
65	8.3KJPN Submission ignored due to conflicting rows: Row 90118971 (NC_000022.10:22844003::A 11402/16760) Row 90118972 (NC_000022.10:22844003:A: 515/16760) Row 90118973 (NC_000022.10:22844003::AA 4/16760)	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 90118971 (NC_000022.10:22844003::A 11402/16760) Row 90118972 (NC_000022.10:22844003:A: 515/16760) Row 90118973 (NC_000022.10:22844003::AA 4/16760)	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 90118971 (NC_000022.10:22844003::A 11402/16760) Row 90118972 (NC_000022.10:22844003:A: 515/16760) Row 90118973 (NC_000022.10:22844003::AA 4/16760)	-	Apr 27, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 126959434 (NC_000022.11:22489678:A: 8060/28258) Row 126959435 (NC_000022.11:22489678:AA: 855/28258) Row 126959437 (NC_000022.11:22489678::A 5/28258)	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 126959434 (NC_000022.11:22489678:A: 8060/28258) Row 126959435 (NC_000022.11:22489678:AA: 855/28258) Row 126959437 (NC_000022.11:22489678::A 5/28258)	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 126959434 (NC_000022.11:22489678:A: 8060/28258) Row 126959435 (NC_000022.11:22489678:AA: 855/28258) Row 126959437 (NC_000022.11:22489678::A 5/28258)	-	Oct 16, 2022 (156)
71	TopMed	NC_000022.11 - 22489679	Apr 27, 2021 (155)
72	ALFA	NC_000022.11 - 22489679	Apr 27, 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)
rs386365946	Aug 21, 2014 (142)
rs143192586	Sep 17, 2011 (135)
rs375874508	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4362862873, ss5310728541, ss5502619812, ss5793122331	NC_000022.11:22489678:AA:	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAA	(self)
3949581486	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAA	(self)
ss5232149665	NC_000022.10:22844003:A:	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	(self)
380802044, ss3645678339, ss3707989614, ss4362862872, ss5105693097, ss5310728540, ss5502619811, ss5793122330, ss5853353629	NC_000022.11:22489678:A:	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	(self)
3949581486	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss104736492	NT_011520.12:2234580:A:	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss4034753028	NT_187629.1:125335:A:	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss256190889, ss327999776, ss328101091, ss328322744, ss552710025, ss553133536, ss553699956, ss1699309524	NC_000022.9:21174003::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss295072900	NC_000022.9:21174007::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss295072901	NC_000022.9:21174010::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss289442238	NC_000022.9:21174013::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
80291901, 31381873, 789307, 19790098, 17125000, ss664517966, ss666767244, ss995240904, ss1378916043, ss1536927274, ss1575812672, ss1809741819, ss3019130952, ss3644458344, ss3685643625, ss3743840135, ss3788799121, ss3793669521, ss3798555870, ss3835936694, ss3841597206, ss5232149664, ss5821927585	NC_000022.10:22844003::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3822420459, ss4362862870, ss5310728542, ss5793122333	NC_000022.11:22489678::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
3949581486	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3707989613	NC_000022.11:22489679::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss193641154	NT_011520.12:2234572::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss95754589, ss288553217	NT_011520.12:2234582::A	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5232149666, ss5981126135	NC_000022.10:22844003::AA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4362862871	NC_000022.11:22489678::AA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3949581486	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAAA	NC_000022.11:22489678:AAAAAAAAAAA:… NC_000022.11:22489678:AAAAAAAAAAA:AAAAAAAAAAAAA	(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 rs75673310

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

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs75673310