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dbSNP Short Genetic Variations

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.

rs79073362

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:69167824-69167841 (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
delTTT / delTT / delT / dupT / dup…

delTTT / delTT / delT / dupT / dupTT / dupTTT

Variation Type
Indel Insertion and Deletion
Frequency
dupT=0.04398 (574/13050, ALFA)
dupT=0.127 (76/600, NorthernSweden)
(T)18=0.5 (4/8, KOREAN) (+ 1 more)
dupT=0.5 (4/8, KOREAN)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
GLCE : 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 13050 TTTTTTTTTTTTTTTTTT=0.95471 TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00130, TTTTTTTTTTTTTTTTTTT=0.04398, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000 0.919023 0.007068 0.073909 32
European Sub 10288 TTTTTTTTTTTTTTTTTT=0.94255 TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00165, TTTTTTTTTTTTTTTTTTT=0.05579, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000 0.897211 0.008972 0.093817 33
African Sub 1706 TTTTTTTTTTTTTTTTTT=1.0000 TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000 1.0 0.0 0.0 N/A
African Others Sub 54 TTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
African American Sub 1652 TTTTTTTTTTTTTTTTTT=1.0000 TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000 1.0 0.0 0.0 N/A
Asian Sub 78 TTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
East Asian Sub 64 TTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 14 TTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 112 TTTTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 446 TTTTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 70 TTTTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Other Sub 350 TTTTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A


Help

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
Allele Frequency Aggregator Total Global 13050 (T)18=0.95471 delTT=0.00000, delT=0.00130, dupT=0.04398, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator European Sub 10288 (T)18=0.94255 delTT=0.00000, delT=0.00165, dupT=0.05579, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator African Sub 1706 (T)18=1.0000 delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator Latin American 2 Sub 446 (T)18=1.000 delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator Other Sub 350 (T)18=1.000 delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator Latin American 1 Sub 112 (T)18=1.000 delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator Asian Sub 78 (T)18=1.00 delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator South Asian Sub 70 (T)18=1.00 delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Northern Sweden ACPOP Study-wide 600 -

No frequency provided

dupT=0.127
KOREAN population from KRGDB KOREAN Study-wide 8 -

No frequency provided

dupT=0.5
Help

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 15 NC_000015.10:g.69167839_69167841del
GRCh38.p14 chr 15 NC_000015.10:g.69167840_69167841del
GRCh38.p14 chr 15 NC_000015.10:g.69167841del
GRCh38.p14 chr 15 NC_000015.10:g.69167841dup
GRCh38.p14 chr 15 NC_000015.10:g.69167840_69167841dup
GRCh38.p14 chr 15 NC_000015.10:g.69167839_69167841dup
GRCh37.p13 chr 15 NC_000015.9:g.69460178_69460180del
GRCh37.p13 chr 15 NC_000015.9:g.69460179_69460180del
GRCh37.p13 chr 15 NC_000015.9:g.69460180del
GRCh37.p13 chr 15 NC_000015.9:g.69460180dup
GRCh37.p13 chr 15 NC_000015.9:g.69460179_69460180dup
GRCh37.p13 chr 15 NC_000015.9:g.69460178_69460180dup
Gene: GLCE, glucuronic acid epimerase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
GLCE transcript variant 2 NM_001324091.2:c.-105+708…

NM_001324091.2:c.-105+7082_-105+7084del

N/A Intron Variant
GLCE transcript variant 3 NM_001324092.2:c.-277+708…

NM_001324092.2:c.-277+7082_-277+7084del

N/A Intron Variant
GLCE transcript variant 4 NM_001324093.2:c.-105+441…

NM_001324093.2:c.-105+4415_-105+4417del

N/A Intron Variant
GLCE transcript variant 5 NM_001324094.2:c.-1232+70…

NM_001324094.2:c.-1232+7082_-1232+7084del

N/A Intron Variant
GLCE transcript variant 1 NM_015554.3:c.-105+7082_-…

NM_015554.3:c.-105+7082_-105+7084del

N/A Intron Variant
GLCE transcript variant X1 XM_047432376.1:c.-867+708…

XM_047432376.1:c.-867+7082_-867+7084del

N/A Intron Variant
GLCE transcript variant X2 XM_047432377.1:c.-1339+70…

XM_047432377.1:c.-1339+7082_-1339+7084del

N/A Intron Variant
GLCE transcript variant X5 XM_047432380.1:c.-867+708…

XM_047432380.1:c.-867+7082_-867+7084del

N/A Intron Variant
GLCE transcript variant X4 XM_017022073.2:c. N/A Genic Upstream Transcript Variant
GLCE transcript variant X6 XM_017022074.3:c. N/A Genic Upstream Transcript Variant
GLCE transcript variant X3 XM_047432379.1:c. N/A Genic Upstream Transcript Variant
Help

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
Help

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 (T)18= delTTT delTT delT dupT dupTT dupTTT
GRCh38.p14 chr 15 NC_000015.10:g.69167824_69167841= NC_000015.10:g.69167839_69167841del NC_000015.10:g.69167840_69167841del NC_000015.10:g.69167841del NC_000015.10:g.69167841dup NC_000015.10:g.69167840_69167841dup NC_000015.10:g.69167839_69167841dup
GRCh37.p13 chr 15 NC_000015.9:g.69460163_69460180= NC_000015.9:g.69460178_69460180del NC_000015.9:g.69460179_69460180del NC_000015.9:g.69460180del NC_000015.9:g.69460180dup NC_000015.9:g.69460179_69460180dup NC_000015.9:g.69460178_69460180dup
GLCE transcript variant 2 NM_001324091.2:c.-105+7067= NM_001324091.2:c.-105+7082_-105+7084del NM_001324091.2:c.-105+7083_-105+7084del NM_001324091.2:c.-105+7084del NM_001324091.2:c.-105+7084dup NM_001324091.2:c.-105+7083_-105+7084dup NM_001324091.2:c.-105+7082_-105+7084dup
GLCE transcript variant 3 NM_001324092.2:c.-277+7067= NM_001324092.2:c.-277+7082_-277+7084del NM_001324092.2:c.-277+7083_-277+7084del NM_001324092.2:c.-277+7084del NM_001324092.2:c.-277+7084dup NM_001324092.2:c.-277+7083_-277+7084dup NM_001324092.2:c.-277+7082_-277+7084dup
GLCE transcript variant 4 NM_001324093.2:c.-105+4400= NM_001324093.2:c.-105+4415_-105+4417del NM_001324093.2:c.-105+4416_-105+4417del NM_001324093.2:c.-105+4417del NM_001324093.2:c.-105+4417dup NM_001324093.2:c.-105+4416_-105+4417dup NM_001324093.2:c.-105+4415_-105+4417dup
GLCE transcript variant 5 NM_001324094.2:c.-1232+7067= NM_001324094.2:c.-1232+7082_-1232+7084del NM_001324094.2:c.-1232+7083_-1232+7084del NM_001324094.2:c.-1232+7084del NM_001324094.2:c.-1232+7084dup NM_001324094.2:c.-1232+7083_-1232+7084dup NM_001324094.2:c.-1232+7082_-1232+7084dup
GLCE transcript NM_015554.1:c.-105+7067= NM_015554.1:c.-105+7082_-105+7084del NM_015554.1:c.-105+7083_-105+7084del NM_015554.1:c.-105+7084del NM_015554.1:c.-105+7084dup NM_015554.1:c.-105+7083_-105+7084dup NM_015554.1:c.-105+7082_-105+7084dup
GLCE transcript variant 1 NM_015554.3:c.-105+7067= NM_015554.3:c.-105+7082_-105+7084del NM_015554.3:c.-105+7083_-105+7084del NM_015554.3:c.-105+7084del NM_015554.3:c.-105+7084dup NM_015554.3:c.-105+7083_-105+7084dup NM_015554.3:c.-105+7082_-105+7084dup
GLCE transcript variant X1 XM_005254298.1:c.-195+7067= XM_005254298.1:c.-195+7082_-195+7084del XM_005254298.1:c.-195+7083_-195+7084del XM_005254298.1:c.-195+7084del XM_005254298.1:c.-195+7084dup XM_005254298.1:c.-195+7083_-195+7084dup XM_005254298.1:c.-195+7082_-195+7084dup
GLCE transcript variant X2 XM_005254299.1:c.-105+7067= XM_005254299.1:c.-105+7082_-105+7084del XM_005254299.1:c.-105+7083_-105+7084del XM_005254299.1:c.-105+7084del XM_005254299.1:c.-105+7084dup XM_005254299.1:c.-105+7083_-105+7084dup XM_005254299.1:c.-105+7082_-105+7084dup
GLCE transcript variant X1 XM_047432376.1:c.-867+7067= XM_047432376.1:c.-867+7082_-867+7084del XM_047432376.1:c.-867+7083_-867+7084del XM_047432376.1:c.-867+7084del XM_047432376.1:c.-867+7084dup XM_047432376.1:c.-867+7083_-867+7084dup XM_047432376.1:c.-867+7082_-867+7084dup
GLCE transcript variant X2 XM_047432377.1:c.-1339+7067= XM_047432377.1:c.-1339+7082_-1339+7084del XM_047432377.1:c.-1339+7083_-1339+7084del XM_047432377.1:c.-1339+7084del XM_047432377.1:c.-1339+7084dup XM_047432377.1:c.-1339+7083_-1339+7084dup XM_047432377.1:c.-1339+7082_-1339+7084dup
GLCE transcript variant X5 XM_047432380.1:c.-867+7067= XM_047432380.1:c.-867+7082_-867+7084del XM_047432380.1:c.-867+7083_-867+7084del XM_047432380.1:c.-867+7084del XM_047432380.1:c.-867+7084dup XM_047432380.1:c.-867+7083_-867+7084dup XM_047432380.1:c.-867+7082_-867+7084dup
Help

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#.

25 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCMHGSC_JDW ss103578172 Dec 01, 2009 (131)
2 SWEGEN ss3013489907 Nov 08, 2017 (151)
3 ACPOP ss3741035004 Jul 13, 2019 (153)
4 EVA ss3834300501 Apr 27, 2020 (154)
5 KRGDB ss3932388614 Apr 27, 2020 (154)
6 KOGIC ss3976399367 Apr 27, 2020 (154)
7 KOGIC ss3976399368 Apr 27, 2020 (154)
8 KOGIC ss3976399369 Apr 27, 2020 (154)
9 GNOMAD ss4291017227 Apr 27, 2021 (155)
10 GNOMAD ss4291017228 Apr 27, 2021 (155)
11 GNOMAD ss4291017229 Apr 27, 2021 (155)
12 GNOMAD ss4291017230 Apr 27, 2021 (155)
13 GNOMAD ss4291017231 Apr 27, 2021 (155)
14 GNOMAD ss4291017232 Apr 27, 2021 (155)
15 TOMMO_GENOMICS ss5216789642 Apr 27, 2021 (155)
16 TOMMO_GENOMICS ss5216789643 Apr 27, 2021 (155)
17 TOMMO_GENOMICS ss5216789644 Apr 27, 2021 (155)
18 1000G_HIGH_COVERAGE ss5298891380 Oct 16, 2022 (156)
19 HUGCELL_USP ss5492576804 Oct 16, 2022 (156)
20 HUGCELL_USP ss5492576805 Oct 16, 2022 (156)
21 HUGCELL_USP ss5492576806 Oct 16, 2022 (156)
22 TOMMO_GENOMICS ss5770772101 Oct 16, 2022 (156)
23 TOMMO_GENOMICS ss5770772102 Oct 16, 2022 (156)
24 TOMMO_GENOMICS ss5770772103 Oct 16, 2022 (156)
25 EVA ss5851347199 Oct 16, 2022 (156)
26 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
27 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
28 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
29 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
30 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
31 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 472823077 (NC_000015.10:69167823::T 17835/125120)
Row 472823078 (NC_000015.10:69167823::TT 1045/125156)
Row 472823079 (NC_000015.10:69167823::TTT 2/125188)...

- Apr 27, 2021 (155)
32 KOREAN population from KRGDB NC_000015.9 - 69460163 Apr 27, 2020 (154)
33 Korean Genome Project

Submission ignored due to conflicting rows:
Row 32777368 (NC_000015.10:69167824::T 340/1832)
Row 32777369 (NC_000015.10:69167824::TT 17/1832)
Row 32777370 (NC_000015.10:69167823:T: 188/1832)

- Apr 27, 2020 (154)
34 Korean Genome Project

Submission ignored due to conflicting rows:
Row 32777368 (NC_000015.10:69167824::T 340/1832)
Row 32777369 (NC_000015.10:69167824::TT 17/1832)
Row 32777370 (NC_000015.10:69167823:T: 188/1832)

- Apr 27, 2020 (154)
35 Korean Genome Project

Submission ignored due to conflicting rows:
Row 32777368 (NC_000015.10:69167824::T 340/1832)
Row 32777369 (NC_000015.10:69167824::TT 17/1832)
Row 32777370 (NC_000015.10:69167823:T: 188/1832)

- Apr 27, 2020 (154)
36 Northern Sweden NC_000015.9 - 69460163 Jul 13, 2019 (153)
37 8.3KJPN

Submission ignored due to conflicting rows:
Row 74758949 (NC_000015.9:69460162::T 3156/16758)
Row 74758950 (NC_000015.9:69460162:T: 32/16758)
Row 74758951 (NC_000015.9:69460162::TT 133/16758)

- Apr 27, 2021 (155)
38 8.3KJPN

Submission ignored due to conflicting rows:
Row 74758949 (NC_000015.9:69460162::T 3156/16758)
Row 74758950 (NC_000015.9:69460162:T: 32/16758)
Row 74758951 (NC_000015.9:69460162::TT 133/16758)

- Apr 27, 2021 (155)
39 8.3KJPN

Submission ignored due to conflicting rows:
Row 74758949 (NC_000015.9:69460162::T 3156/16758)
Row 74758950 (NC_000015.9:69460162:T: 32/16758)
Row 74758951 (NC_000015.9:69460162::TT 133/16758)

- Apr 27, 2021 (155)
40 14KJPN

Submission ignored due to conflicting rows:
Row 104609205 (NC_000015.10:69167823::TT 229/28258)
Row 104609206 (NC_000015.10:69167823::T 5319/28258)
Row 104609207 (NC_000015.10:69167823:T: 34/28258)

- Oct 16, 2022 (156)
41 14KJPN

Submission ignored due to conflicting rows:
Row 104609205 (NC_000015.10:69167823::TT 229/28258)
Row 104609206 (NC_000015.10:69167823::T 5319/28258)
Row 104609207 (NC_000015.10:69167823:T: 34/28258)

- Oct 16, 2022 (156)
42 14KJPN

Submission ignored due to conflicting rows:
Row 104609205 (NC_000015.10:69167823::TT 229/28258)
Row 104609206 (NC_000015.10:69167823::T 5319/28258)
Row 104609207 (NC_000015.10:69167823:T: 34/28258)

- Oct 16, 2022 (156)
43 ALFA NC_000015.10 - 69167824 Apr 27, 2021 (155)
Help

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
ss4291017232 NC_000015.10:69167823:TTT: NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss103578172 NT_010194.17:40250734:TTT: NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss4291017231 NC_000015.10:69167823:TT: NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
10231821235 NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
ss3013489907, ss5216789643 NC_000015.9:69460162:T: NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss3976399369, ss4291017230, ss5298891380, ss5492576806, ss5770772103, ss5851347199 NC_000015.10:69167823:T: NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
10231821235 NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
39566008, 14319869, ss3741035004, ss3834300501, ss3932388614, ss5216789642 NC_000015.9:69460162::T NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss4291017227, ss5492576804, ss5770772102 NC_000015.10:69167823::T NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
10231821235 NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss3976399367 NC_000015.10:69167824::T NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss5216789644 NC_000015.9:69460162::TT NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss4291017228, ss5492576805, ss5770772101 NC_000015.10:69167823::TT NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
10231821235 NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss3976399368 NC_000015.10:69167824::TT NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss4291017229 NC_000015.10:69167823::TTT NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
10231821235 NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

NC_000015.10:69167823:TTTTTTTTTTTT…

NC_000015.10:69167823:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs79073362

Help

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.

Software version is: 2.0.1.post820+afb47a3d