Name: rs765351246
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.

rs765351246

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:14230972-14230976 (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(G)₄ / delGG
Variation Type: Indel Insertion and Deletion
Frequency: del(G)₄=0.096714 (13481/139390, GnomAD)
del(G)₄=0.25593 (7232/28258, 14KJPN)
del(G)₄=0.25394 (4256/16760, 8.3KJPN) (+ 9 more)
delGG=0.07384 (1206/16332, ALFA)
del(G)₄=0.1060 (679/6404, 1000G_30x)
delGG=0.1092 (547/5008, 1000G)
del(G)₄=0.1002 (449/4480, Estonian)
delGG=0.1253 (483/3854, ALSPAC)
delGG=0.1224 (454/3708, TWINSUK)
del(G)₄=0.2058 (377/1832, Korea1K)
del(G)₄=0.147 (88/600, NorthernSweden)
del(G)₄=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NFIB : 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	16332	GGGGG=0.89873	G=0.02743, GGG=0.07384	0.853101	0.008915	0.137984	7
European	Sub	12080	GGGGG=0.88452	G=0.03700, GGG=0.07848	0.84114	0.009973	0.148887	5
African	Sub	2816	GGGGG=0.9737	G=0.0000, GGG=0.0263	0.948153	0.00071	0.051136	0
African Others	Sub	108	GGGGG=0.972	G=0.000, GGG=0.028	0.944444	0.0	0.055556	0
African American	Sub	2708	GGGGG=0.9738	G=0.0000, GGG=0.0262	0.948301	0.000739	0.05096	0
Asian	Sub	108	GGGGG=0.861	G=0.000, GGG=0.139	0.722222	0.0	0.277778	1
East Asian	Sub	84	GGGGG=0.85	G=0.00, GGG=0.15	0.690476	0.0	0.309524	1
Other Asian	Sub	24	GGGGG=0.92	G=0.00, GGG=0.08	0.833333	0.0	0.166667	0
Latin American 1	Sub	146	GGGGG=0.884	G=0.000, GGG=0.116	0.780822	0.013699	0.205479	0
Latin American 2	Sub	610	GGGGG=0.877	G=0.000, GGG=0.123	0.777049	0.022951	0.2	1
South Asian	Sub	94	GGGGG=0.81	G=0.00, GGG=0.19	0.617021	0.0	0.382979	2
Other	Sub	478	GGGGG=0.874	G=0.002, GGG=0.123	0.768908	0.016807	0.214286	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
gnomAD - Genomes	Global	Study-wide	139390	(G)₅=0.903286	del(G)₄=0.096714
gnomAD - Genomes	European	Sub	75516	(G)₅=0.87178	del(G)₄=0.12822
gnomAD - Genomes	African	Sub	41748	(G)₅=0.97157	del(G)₄=0.02843
gnomAD - Genomes	American	Sub	13570	(G)₅=0.89108	del(G)₄=0.10892
gnomAD - Genomes	Ashkenazi Jewish	Sub	3308	(G)₅=0.8482	del(G)₄=0.1518
gnomAD - Genomes	East Asian	Sub	3112	(G)₅=0.8596	del(G)₄=0.1404
gnomAD - Genomes	Other	Sub	2136	(G)₅=0.9092	del(G)₄=0.0908
14KJPN	JAPANESE	Study-wide	28258	(G)₅=0.74407	del(G)₄=0.25593
8.3KJPN	JAPANESE	Study-wide	16760	(G)₅=0.74606	del(G)₄=0.25394
Allele Frequency Aggregator	Total	Global	16332	(G)₅=0.89873	del(G)₄=0.02743, delGG=0.07384
Allele Frequency Aggregator	European	Sub	12080	(G)₅=0.88452	del(G)₄=0.03700, delGG=0.07848
Allele Frequency Aggregator	African	Sub	2816	(G)₅=0.9737	del(G)₄=0.0000, delGG=0.0263
Allele Frequency Aggregator	Latin American 2	Sub	610	(G)₅=0.877	del(G)₄=0.000, delGG=0.123
Allele Frequency Aggregator	Other	Sub	478	(G)₅=0.874	del(G)₄=0.002, delGG=0.123
Allele Frequency Aggregator	Latin American 1	Sub	146	(G)₅=0.884	del(G)₄=0.000, delGG=0.116
Allele Frequency Aggregator	Asian	Sub	108	(G)₅=0.861	del(G)₄=0.000, delGG=0.139
Allele Frequency Aggregator	South Asian	Sub	94	(G)₅=0.81	del(G)₄=0.00, delGG=0.19
1000Genomes_30x	Global	Study-wide	6404	(G)₅=0.8940	del(G)₄=0.1060
1000Genomes_30x	African	Sub	1786	(G)₅=0.9894	del(G)₄=0.0106
1000Genomes_30x	Europe	Sub	1266	(G)₅=0.8768	del(G)₄=0.1232
1000Genomes_30x	South Asian	Sub	1202	(G)₅=0.8253	del(G)₄=0.1747
1000Genomes_30x	East Asian	Sub	1170	(G)₅=0.8607	del(G)₄=0.1393
1000Genomes_30x	American	Sub	980	(G)₅=0.866	del(G)₄=0.134
1000Genomes	Global	Study-wide	5008	(G)₅=0.8908	delGG=0.1092
1000Genomes	African	Sub	1322	(G)₅=0.9879	delGG=0.0121
1000Genomes	East Asian	Sub	1008	(G)₅=0.8641	delGG=0.1359
1000Genomes	Europe	Sub	1006	(G)₅=0.8797	delGG=0.1203
1000Genomes	South Asian	Sub	978	(G)₅=0.812	delGG=0.188
1000Genomes	American	Sub	694	(G)₅=0.872	delGG=0.128
Genetic variation in the Estonian population	Estonian	Study-wide	4480	(G)₅=0.8998	del(G)₄=0.1002
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(G)₅=0.8747	delGG=0.1253
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(G)₅=0.8776	delGG=0.1224
Korean Genome Project	KOREAN	Study-wide	1832	(G)₅=0.7942	del(G)₄=0.2058
Northern Sweden	ACPOP	Study-wide	600	(G)₅=0.853	del(G)₄=0.147
The Danish reference pan genome	Danish	Study-wide	40	(G)₅=0.93	del(G)₄=0.07

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 9	NC_000009.12:g.14230973_14230976del
GRCh38.p14 chr 9	NC_000009.12:g.14230975_14230976del
GRCh37.p13 chr 9	NC_000009.11:g.14230972_14230975del
GRCh37.p13 chr 9	NC_000009.11:g.14230974_14230975del

Gene: NFIB, nuclear factor I B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NFIB transcript variant 1	NM_001190737.2:c.563-5119… NM_001190737.2:c.563-51195_563-51192del	N/A	Intron Variant
NFIB transcript variant 2	NM_001190738.2:c.641-5119… NM_001190738.2:c.641-51195_641-51192del	N/A	Intron Variant
NFIB transcript variant 5	NM_001369458.1:c.629-5119… NM_001369458.1:c.629-51195_629-51192del	N/A	Intron Variant
NFIB transcript variant 6	NM_001369459.1:c.629-5119… NM_001369459.1:c.629-51195_629-51192del	N/A	Intron Variant
NFIB transcript variant 7	NM_001369460.1:c.551-5119… NM_001369460.1:c.551-51195_551-51192del	N/A	Intron Variant
NFIB transcript variant 8	NM_001369461.1:c.563-5119… NM_001369461.1:c.563-51195_563-51192del	N/A	Intron Variant
NFIB transcript variant 9	NM_001369462.1:c.629-5119… NM_001369462.1:c.629-51195_629-51192del	N/A	Intron Variant
NFIB transcript variant 10	NM_001369463.1:c.551-5119… NM_001369463.1:c.551-51195_551-51192del	N/A	Intron Variant
NFIB transcript variant 11	NM_001369464.1:c.563-5119… NM_001369464.1:c.563-51195_563-51192del	N/A	Intron Variant
NFIB transcript variant 12	NM_001369465.1:c.536-5119… NM_001369465.1:c.536-51195_536-51192del	N/A	Intron Variant
NFIB transcript variant 13	NM_001369466.1:c.551-5119… NM_001369466.1:c.551-51195_551-51192del	N/A	Intron Variant
NFIB transcript variant 14	NM_001369467.1:c.536-5119… NM_001369467.1:c.536-51195_536-51192del	N/A	Intron Variant
NFIB transcript variant 15	NM_001369468.1:c.629-5119… NM_001369468.1:c.629-51195_629-51192del	N/A	Intron Variant
NFIB transcript variant 16	NM_001369469.1:c.419-5119… NM_001369469.1:c.419-51195_419-51192del	N/A	Intron Variant
NFIB transcript variant 17	NM_001369470.1:c.326-5119… NM_001369470.1:c.326-51195_326-51192del	N/A	Intron Variant
NFIB transcript variant 18	NM_001369471.1:c.563-5119… NM_001369471.1:c.563-51195_563-51192del	N/A	Intron Variant
NFIB transcript variant 19	NM_001369472.1:c.551-5119… NM_001369472.1:c.551-51195_551-51192del	N/A	Intron Variant
NFIB transcript variant 20	NM_001369473.1:c.551-5119… NM_001369473.1:c.551-51195_551-51192del	N/A	Intron Variant
NFIB transcript variant 21	NM_001369474.1:c.548-5119… NM_001369474.1:c.548-51195_548-51192del	N/A	Intron Variant
NFIB transcript variant 22	NM_001369475.1:c.338-5119… NM_001369475.1:c.338-51195_338-51192del	N/A	Intron Variant
NFIB transcript variant 23	NM_001369476.1:c.536-5119… NM_001369476.1:c.536-51195_536-51192del	N/A	Intron Variant
NFIB transcript variant 24	NM_001369477.1:c.563-7508… NM_001369477.1:c.563-75082_563-75079del	N/A	Intron Variant
NFIB transcript variant 25	NM_001369478.1:c.326-5119… NM_001369478.1:c.326-51195_326-51192del	N/A	Intron Variant
NFIB transcript variant 26	NM_001369479.1:c.26-51195… NM_001369479.1:c.26-51195_26-51192del	N/A	Intron Variant
NFIB transcript variant 27	NM_001369480.1:c.26-51195… NM_001369480.1:c.26-51195_26-51192del	N/A	Intron Variant
NFIB transcript variant 3	NM_005596.3:c.563-51195_5… NM_005596.3:c.563-51195_563-51192del	N/A	Intron Variant
NFIB transcript variant 4	NM_001282787.2:c.	N/A	Genic Upstream Transcript Variant
NFIB transcript variant 28	NM_001369481.1:c.	N/A	Genic Downstream Transcript Variant
NFIB transcript variant 29	NR_161382.1:n.	N/A	Intron Variant
NFIB transcript variant 30	NR_161383.1:n.	N/A	Intron Variant
NFIB transcript variant 31	NR_161384.1:n.	N/A	Intron Variant
NFIB transcript variant 32	NR_161385.1:n.	N/A	Genic Upstream Transcript 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	(G)₅=	del(G)₄	delGG
GRCh38.p14 chr 9	NC_000009.12:g.14230972_14230976=	NC_000009.12:g.14230973_14230976del	NC_000009.12:g.14230975_14230976del
GRCh37.p13 chr 9	NC_000009.11:g.14230971_14230975=	NC_000009.11:g.14230972_14230975del	NC_000009.11:g.14230974_14230975del
NFIB transcript variant 1	NM_001190737.1:c.563-51192=	NM_001190737.1:c.563-51195_563-51192del	NM_001190737.1:c.563-51193_563-51192del
NFIB transcript variant 1	NM_001190737.2:c.563-51192=	NM_001190737.2:c.563-51195_563-51192del	NM_001190737.2:c.563-51193_563-51192del
NFIB transcript variant 2	NM_001190738.1:c.641-51192=	NM_001190738.1:c.641-51195_641-51192del	NM_001190738.1:c.641-51193_641-51192del
NFIB transcript variant 2	NM_001190738.2:c.641-51192=	NM_001190738.2:c.641-51195_641-51192del	NM_001190738.2:c.641-51193_641-51192del
NFIB transcript variant 5	NM_001369458.1:c.629-51192=	NM_001369458.1:c.629-51195_629-51192del	NM_001369458.1:c.629-51193_629-51192del
NFIB transcript variant 6	NM_001369459.1:c.629-51192=	NM_001369459.1:c.629-51195_629-51192del	NM_001369459.1:c.629-51193_629-51192del
NFIB transcript variant 7	NM_001369460.1:c.551-51192=	NM_001369460.1:c.551-51195_551-51192del	NM_001369460.1:c.551-51193_551-51192del
NFIB transcript variant 8	NM_001369461.1:c.563-51192=	NM_001369461.1:c.563-51195_563-51192del	NM_001369461.1:c.563-51193_563-51192del
NFIB transcript variant 9	NM_001369462.1:c.629-51192=	NM_001369462.1:c.629-51195_629-51192del	NM_001369462.1:c.629-51193_629-51192del
NFIB transcript variant 10	NM_001369463.1:c.551-51192=	NM_001369463.1:c.551-51195_551-51192del	NM_001369463.1:c.551-51193_551-51192del
NFIB transcript variant 11	NM_001369464.1:c.563-51192=	NM_001369464.1:c.563-51195_563-51192del	NM_001369464.1:c.563-51193_563-51192del
NFIB transcript variant 12	NM_001369465.1:c.536-51192=	NM_001369465.1:c.536-51195_536-51192del	NM_001369465.1:c.536-51193_536-51192del
NFIB transcript variant 13	NM_001369466.1:c.551-51192=	NM_001369466.1:c.551-51195_551-51192del	NM_001369466.1:c.551-51193_551-51192del
NFIB transcript variant 14	NM_001369467.1:c.536-51192=	NM_001369467.1:c.536-51195_536-51192del	NM_001369467.1:c.536-51193_536-51192del
NFIB transcript variant 15	NM_001369468.1:c.629-51192=	NM_001369468.1:c.629-51195_629-51192del	NM_001369468.1:c.629-51193_629-51192del
NFIB transcript variant 16	NM_001369469.1:c.419-51192=	NM_001369469.1:c.419-51195_419-51192del	NM_001369469.1:c.419-51193_419-51192del
NFIB transcript variant 17	NM_001369470.1:c.326-51192=	NM_001369470.1:c.326-51195_326-51192del	NM_001369470.1:c.326-51193_326-51192del
NFIB transcript variant 18	NM_001369471.1:c.563-51192=	NM_001369471.1:c.563-51195_563-51192del	NM_001369471.1:c.563-51193_563-51192del
NFIB transcript variant 19	NM_001369472.1:c.551-51192=	NM_001369472.1:c.551-51195_551-51192del	NM_001369472.1:c.551-51193_551-51192del
NFIB transcript variant 20	NM_001369473.1:c.551-51192=	NM_001369473.1:c.551-51195_551-51192del	NM_001369473.1:c.551-51193_551-51192del
NFIB transcript variant 21	NM_001369474.1:c.548-51192=	NM_001369474.1:c.548-51195_548-51192del	NM_001369474.1:c.548-51193_548-51192del
NFIB transcript variant 22	NM_001369475.1:c.338-51192=	NM_001369475.1:c.338-51195_338-51192del	NM_001369475.1:c.338-51193_338-51192del
NFIB transcript variant 23	NM_001369476.1:c.536-51192=	NM_001369476.1:c.536-51195_536-51192del	NM_001369476.1:c.536-51193_536-51192del
NFIB transcript variant 24	NM_001369477.1:c.563-75079=	NM_001369477.1:c.563-75082_563-75079del	NM_001369477.1:c.563-75080_563-75079del
NFIB transcript variant 25	NM_001369478.1:c.326-51192=	NM_001369478.1:c.326-51195_326-51192del	NM_001369478.1:c.326-51193_326-51192del
NFIB transcript variant 26	NM_001369479.1:c.26-51192=	NM_001369479.1:c.26-51195_26-51192del	NM_001369479.1:c.26-51193_26-51192del
NFIB transcript variant 27	NM_001369480.1:c.26-51192=	NM_001369480.1:c.26-51195_26-51192del	NM_001369480.1:c.26-51193_26-51192del
NFIB transcript variant 3	NM_005596.3:c.563-51192=	NM_005596.3:c.563-51195_563-51192del	NM_005596.3:c.563-51193_563-51192del
NFIB transcript variant X1	XM_005251467.1:c.563-51192=	XM_005251467.1:c.563-51195_563-51192del	XM_005251467.1:c.563-51193_563-51192del
NFIB transcript variant X2	XM_005251468.1:c.551-51192=	XM_005251468.1:c.551-51195_551-51192del	XM_005251468.1:c.551-51193_551-51192del
NFIB transcript variant X4	XM_005251469.1:c.563-51192=	XM_005251469.1:c.563-51195_563-51192del	XM_005251469.1:c.563-51193_563-51192del
NFIB transcript variant X7	XM_005251470.1:c.563-51192=	XM_005251470.1:c.563-51195_563-51192del	XM_005251470.1:c.563-51193_563-51192del

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#.

29 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss663907944	Jan 10, 2018 (151)
2	SSIP	ss947234669	Jan 10, 2018 (151)
3	1000GENOMES	ss1368173603	Jan 10, 2018 (151)
4	EVA_GENOME_DK	ss1577338420	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1706335005	Jan 10, 2018 (151)
6	EVA_UK10K_TWINSUK	ss1706335006	Jan 10, 2018 (151)
7	GENOMED	ss1971162561	Jul 19, 2016 (147)
8	JJLAB	ss2030953211	Sep 14, 2016 (149)
9	GNOMAD	ss2875762422	Nov 08, 2017 (151)
10	SWEGEN	ss3004432194	Nov 08, 2017 (151)
11	EGCUT_WGS	ss3672173874	Jul 13, 2019 (153)
12	EVA_DECODE	ss3723533990	Jul 13, 2019 (153)
13	ACPOP	ss3736336126	Jul 13, 2019 (153)
14	PACBIO	ss3786356082	Jul 13, 2019 (153)
15	PACBIO	ss3791580978	Jul 13, 2019 (153)
16	PACBIO	ss3796462636	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3812111955	Jul 13, 2019 (153)
18	EVA	ss3831552883	Apr 26, 2020 (154)
19	KOGIC	ss3965354088	Apr 26, 2020 (154)
20	TOMMO_GENOMICS	ss5192214789	Apr 26, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5279898703	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5476170533	Oct 16, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5571722384	Oct 16, 2022 (156)
24	SANFORD_IMAGENETICS	ss5646966502	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5735300060	Oct 16, 2022 (156)
26	YY_MCH	ss5810369900	Oct 16, 2022 (156)
27	EVA	ss5828891864	Oct 16, 2022 (156)
28	EVA	ss5915644534	Oct 16, 2022 (156)
29	EVA	ss5976240087	Oct 16, 2022 (156)
30	1000Genomes	NC_000009.11 - 14230971	Oct 12, 2018 (152)
31	1000Genomes_30x	NC_000009.12 - 14230972	Oct 16, 2022 (156)
32	The Avon Longitudinal Study of Parents and Children	NC_000009.11 - 14230971	Oct 12, 2018 (152)
33	Genetic variation in the Estonian population	NC_000009.11 - 14230971	Oct 12, 2018 (152)
34	The Danish reference pan genome	NC_000009.11 - 14230971	Apr 26, 2020 (154)
35	gnomAD - Genomes	NC_000009.12 - 14230972	Apr 26, 2021 (155)
36	Korean Genome Project	NC_000009.12 - 14230972	Apr 26, 2020 (154)
37	Northern Sweden	NC_000009.11 - 14230971	Jul 13, 2019 (153)
38	8.3KJPN	NC_000009.11 - 14230971	Apr 26, 2021 (155)
39	14KJPN	NC_000009.12 - 14230972	Oct 16, 2022 (156)
40	UK 10K study - Twins	NC_000009.11 - 14230971	Oct 12, 2018 (152)
41	ALFA	NC_000009.12 - 14230972	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
17912122, 1264285, 9620991, 50184096, ss1577338420, ss1971162561, ss2030953211, ss2875762422, ss3004432194, ss3672173874, ss3736336126, ss3786356082, ss3831552883, ss5192214789, ss5646966502	NC_000009.11:14230970:GGGG:	NC_000009.12:14230971:GGGGG:G	(self)
59248319, 318974741, 21732089, 69137164, ss3723533990, ss3965354088, ss5279898703, ss5476170533, ss5571722384, ss5735300060, ss5810369900	NC_000009.12:14230971:GGGG:	NC_000009.12:14230971:GGGGG:G	(self)
11341458642	NC_000009.12:14230971:GGGGG:G	NC_000009.12:14230971:GGGGG:G	(self)
45253201, 25177844, 25177844, ss663907944, ss947234669, ss1368173603, ss1706335005, ss1706335006, ss3791580978, ss3796462636, ss5828891864, ss5976240087	NC_000009.11:14230970:GG:	NC_000009.12:14230971:GGGGG:GGG	(self)
ss3812111955, ss5915644534	NC_000009.12:14230971:GG:	NC_000009.12:14230971:GGGGG:GGG	(self)
11341458642	NC_000009.12:14230971:GGGGG:GGG	NC_000009.12:14230971:GGGGG:GGG	(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 rs765351246

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

rs765351246