Name: rs782627895
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.

rs782627895

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:149772147-149772161 (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(C)₆ / del(C)₅ / del(C)₄ / delC…
del(C)₆ / del(C)₅ / del(C)₄ / delCC / delC / dupC / dupCC / dupCCC
Variation Type: Indel Insertion and Deletion
Frequency: dupC=0.02409 (265/11002, ALFA)
(C)₁₅=0.0752 (279/3708, TWINSUK)
(C)₁₅=0.0630 (182/2889, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HSFX1 : 2KB Upstream 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	11002	CCCCCCCCCCCCCCC=0.96273	CCCCCCCCCC=0.00000, CCCCCCCCCCC=0.00000, CCCCCCCCCCCCC=0.00000, CCCCCCCCCCCCCC=0.01300, CCCCCCCCCCCCCCCC=0.02409, CCCCCCCCCCCCCCCCC=0.00018	0.973179	0.020302	0.006519	32
European	Sub	8622	CCCCCCCCCCCCCCC=0.9524	CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0166, CCCCCCCCCCCCCCCC=0.0307, CCCCCCCCCCCCCCCCC=0.0002	0.965542	0.026083	0.008375	32
African	Sub	1508	CCCCCCCCCCCCCCC=1.0000	CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	68	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	1440	CCCCCCCCCCCCCCC=1.0000	CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.0000, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCCCCC=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	60	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	48	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	94	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	316	CCCCCCCCCCCCCCC=1.000	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	74	CCCCCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	328	CCCCCCCCCCCCCCC=1.000	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCCCC=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	11002	(C)₁₅=0.96273	del(C)₅=0.00000, del(C)₄=0.00000, delCC=0.00000, delC=0.01300, dupC=0.02409, dupCC=0.00018
Allele Frequency Aggregator	European	Sub	8622	(C)₁₅=0.9524	del(C)₅=0.0000, del(C)₄=0.0000, delCC=0.0000, delC=0.0166, dupC=0.0307, dupCC=0.0002
Allele Frequency Aggregator	African	Sub	1508	(C)₁₅=1.0000	del(C)₅=0.0000, del(C)₄=0.0000, delCC=0.0000, delC=0.0000, dupC=0.0000, dupCC=0.0000
Allele Frequency Aggregator	Other	Sub	328	(C)₁₅=1.000	del(C)₅=0.000, del(C)₄=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	316	(C)₁₅=1.000	del(C)₅=0.000, del(C)₄=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	94	(C)₁₅=1.00	del(C)₅=0.00, del(C)₄=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	South Asian	Sub	74	(C)₁₅=1.00	del(C)₅=0.00, del(C)₄=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
Allele Frequency Aggregator	Asian	Sub	60	(C)₁₅=1.00	del(C)₅=0.00, del(C)₄=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupCCC=0.9248
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	2889	- No frequency provided	dupCCC=0.9370

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 X	NC_000023.11:g.149772156_149772161del
GRCh38.p14 chr X	NC_000023.11:g.149772157_149772161del
GRCh38.p14 chr X	NC_000023.11:g.149772158_149772161del
GRCh38.p14 chr X	NC_000023.11:g.149772160_149772161del
GRCh38.p14 chr X	NC_000023.11:g.149772161del
GRCh38.p14 chr X	NC_000023.11:g.149772161dup
GRCh38.p14 chr X	NC_000023.11:g.149772160_149772161dup
GRCh38.p14 chr X	NC_000023.11:g.149772159_149772161dup
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296554_5296559del
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296555_5296559del
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296556_5296559del
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296558_5296559del
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296559del
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296559dup
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296558_5296559dup
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296557_5296559dup
TMEM185AP1 pseudogene	NG_029343.2:g.3374_3379del
TMEM185AP1 pseudogene	NG_029343.2:g.3375_3379del
TMEM185AP1 pseudogene	NG_029343.2:g.3376_3379del
TMEM185AP1 pseudogene	NG_029343.2:g.3378_3379del
TMEM185AP1 pseudogene	NG_029343.2:g.3379del
TMEM185AP1 pseudogene	NG_029343.2:g.3379dup
TMEM185AP1 pseudogene	NG_029343.2:g.3378_3379dup
TMEM185AP1 pseudogene	NG_029343.2:g.3377_3379dup
GRCh37.p13 chr X	NC_000023.10:g.148853817_148853819dup
GRCh37.p13 chr X	NC_000023.10:g.148853817_148853819del
GRCh37.p13 chr X	NC_000023.10:g.148853818_148853819del
GRCh37.p13 chr X	NC_000023.10:g.148853819del
GRCh37.p13 chr X	NC_000023.10:g.148853819dup
GRCh37.p13 chr X	NC_000023.10:g.148853818_148853819dup
GRCh37.p13 chr X	NC_000023.10:g.148853816_148853819dup
GRCh37.p13 chr X	NC_000023.10:g.148853815_148853819dup
GRCh37.p13 chr X	NC_000023.10:g.148853814_148853819dup

Gene: HSFX1, heat shock transcription factor family, X-linked 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
HSFX1 transcript	NM_016153.3:c.	N/A	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	(C)₁₅=	del(C)₆	del(C)₅	del(C)₄	delCC	delC	dupC	dupCC	dupCCC
GRCh38.p14 chr X	NC_000023.11:g.149772147_149772161=	NC_000023.11:g.149772156_149772161del	NC_000023.11:g.149772157_149772161del	NC_000023.11:g.149772158_149772161del	NC_000023.11:g.149772160_149772161del	NC_000023.11:g.149772161del	NC_000023.11:g.149772161dup	NC_000023.11:g.149772160_149772161dup	NC_000023.11:g.149772159_149772161dup
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5296545_5296559=	NW_004070890.2:g.5296554_5296559del	NW_004070890.2:g.5296555_5296559del	NW_004070890.2:g.5296556_5296559del	NW_004070890.2:g.5296558_5296559del	NW_004070890.2:g.5296559del	NW_004070890.2:g.5296559dup	NW_004070890.2:g.5296558_5296559dup	NW_004070890.2:g.5296557_5296559dup
TMEM185AP1 pseudogene	NG_029343.2:g.3365_3379=	NG_029343.2:g.3374_3379del	NG_029343.2:g.3375_3379del	NG_029343.2:g.3376_3379del	NG_029343.2:g.3378_3379del	NG_029343.2:g.3379del	NG_029343.2:g.3379dup	NG_029343.2:g.3378_3379dup	NG_029343.2:g.3377_3379dup
GRCh37.p13 chr X	NC_000023.10:g.148853817_148853819dup	NC_000023.10:g.148853817_148853819del	NC_000023.10:g.148853818_148853819del	NC_000023.10:g.148853819del	NC_000023.10:g.148853819dup	NC_000023.10:g.148853818_148853819dup	NC_000023.10:g.148853816_148853819dup	NC_000023.10:g.148853815_148853819dup	NC_000023.10:g.148853814_148853819dup

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#.

24 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_UK10K_ALSPAC	ss1709895652	Apr 09, 2015 (144)
2	EVA_UK10K_TWINSUK	ss1709895745	Apr 09, 2015 (144)
3	MCHAISSO	ss3065280998	Nov 08, 2017 (151)
4	MCHAISSO	ss3066314281	Nov 08, 2017 (151)
5	GNOMAD	ss4380667204	Apr 27, 2021 (155)
6	GNOMAD	ss4380667205	Apr 27, 2021 (155)
7	GNOMAD	ss4380667206	Apr 27, 2021 (155)
8	GNOMAD	ss4380667207	Apr 27, 2021 (155)
9	GNOMAD	ss4380667208	Apr 27, 2021 (155)
10	GNOMAD	ss4380667209	Apr 27, 2021 (155)
11	TOMMO_GENOMICS	ss5236708237	Apr 27, 2021 (155)
12	TOMMO_GENOMICS	ss5236708238	Apr 27, 2021 (155)
13	TOMMO_GENOMICS	ss5236708239	Apr 27, 2021 (155)
14	TOMMO_GENOMICS	ss5236708240	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5236708241	Apr 27, 2021 (155)
16	HUGCELL_USP	ss5505644741	Oct 13, 2022 (156)
17	HUGCELL_USP	ss5505644742	Oct 13, 2022 (156)
18	SANFORD_IMAGENETICS	ss5666058441	Oct 13, 2022 (156)
19	TOMMO_GENOMICS	ss5799210830	Oct 13, 2022 (156)
20	TOMMO_GENOMICS	ss5799210831	Oct 13, 2022 (156)
21	TOMMO_GENOMICS	ss5799210832	Oct 13, 2022 (156)
22	TOMMO_GENOMICS	ss5799210833	Oct 13, 2022 (156)
23	TOMMO_GENOMICS	ss5799210834	Oct 13, 2022 (156)
24	EVA	ss5979202571	Oct 13, 2022 (156)
25	The Avon Longitudinal Study of Parents and Children	NC_000023.10 - 148853808	Oct 13, 2018 (152)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 593948741 (NC_000023.11:149772146::C 1/2093) Row 593948742 (NC_000023.11:149772146:C: 53/2062) Row 593948743 (NC_000023.11:149772146:CC: 484/2059)...	-	Apr 27, 2021 (155)
32	8.3KJPN Submission ignored due to conflicting rows: Row 94677544 (NC_000023.10:148853807::C 2323/9074) Row 94677545 (NC_000023.10:148853807:C: 119/9074) Row 94677546 (NC_000023.10:148853807:CC: 1/9074)...	-	Apr 27, 2021 (155)
33	8.3KJPN Submission ignored due to conflicting rows: Row 94677544 (NC_000023.10:148853807::C 2323/9074) Row 94677545 (NC_000023.10:148853807:C: 119/9074) Row 94677546 (NC_000023.10:148853807:CC: 1/9074)...	-	Apr 27, 2021 (155)
34	8.3KJPN Submission ignored due to conflicting rows: Row 94677544 (NC_000023.10:148853807::C 2323/9074) Row 94677545 (NC_000023.10:148853807:C: 119/9074) Row 94677546 (NC_000023.10:148853807:CC: 1/9074)...	-	Apr 27, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 94677544 (NC_000023.10:148853807::C 2323/9074) Row 94677545 (NC_000023.10:148853807:C: 119/9074) Row 94677546 (NC_000023.10:148853807:CC: 1/9074)...	-	Apr 27, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 94677544 (NC_000023.10:148853807::C 2323/9074) Row 94677545 (NC_000023.10:148853807:C: 119/9074) Row 94677546 (NC_000023.10:148853807:CC: 1/9074)...	-	Apr 27, 2021 (155)
37	14KJPN Submission ignored due to conflicting rows: Row 133047934 (NC_000023.11:149772146:CCCC: 796/8359) Row 133047935 (NC_000023.11:149772146:CC: 460/8359) Row 133047936 (NC_000023.11:149772146:CCCCC: 51/8359)...	-	Oct 13, 2022 (156)
38	14KJPN Submission ignored due to conflicting rows: Row 133047934 (NC_000023.11:149772146:CCCC: 796/8359) Row 133047935 (NC_000023.11:149772146:CC: 460/8359) Row 133047936 (NC_000023.11:149772146:CCCCC: 51/8359)...	-	Oct 13, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 133047934 (NC_000023.11:149772146:CCCC: 796/8359) Row 133047935 (NC_000023.11:149772146:CC: 460/8359) Row 133047936 (NC_000023.11:149772146:CCCCC: 51/8359)...	-	Oct 13, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 133047934 (NC_000023.11:149772146:CCCC: 796/8359) Row 133047935 (NC_000023.11:149772146:CC: 460/8359) Row 133047936 (NC_000023.11:149772146:CCCCC: 51/8359)...	-	Oct 13, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 133047934 (NC_000023.11:149772146:CCCC: 796/8359) Row 133047935 (NC_000023.11:149772146:CC: 460/8359) Row 133047936 (NC_000023.11:149772146:CCCCC: 51/8359)...	-	Oct 13, 2022 (156)
42	UK 10K study - Twins	NC_000023.10 - 148853808	Oct 13, 2018 (152)
43	ALFA	NC_000023.11 - 149772147	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4380667209	NC_000023.11:149772146:CCCCCC:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCC	(self)
ss4380667208, ss5799210832	NC_000023.11:149772146:CCCCC:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCC	(self)
ss3065280998, ss3066314281, ss4380667207, ss5799210830	NC_000023.11:149772146:CCCC:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss5236708239	NC_000023.10:148853807:CC:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4380667206, ss5505644741, ss5799210831	NC_000023.11:149772146:CC:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss5236708238, ss5666058441	NC_000023.10:148853807:C:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4380667205, ss5505644742, ss5799210834	NC_000023.11:149772146:C:	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss5236708237	NC_000023.10:148853807::C	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)
ss4380667204, ss5799210833	NC_000023.11:149772146::C	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)
ss5236708240	NC_000023.10:148853807::CC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCCC	(self)
13534597818	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCCC	(self)
46561336, 46561336, ss1709895652, ss1709895745, ss5236708241, ss5979202571	NC_000023.10:148853807::CCC	NC_000023.11:149772146:CCCCCCCCCCC… NC_000023.11:149772146:CCCCCCCCCCCCCCC:CCCCCCCCCCCCCCCCCC	(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 rs782627895

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

rs782627895