SNP Links for Nucleotide (Select 223718450) - SNP

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Links from Nucleotide

Items: 1 to 20 of 274

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Select item 14909707321.

rs1490970732 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:49899026 (GRCh38)
11:49920578 (GRCh37)
Canonical SPDI:: NC_000011.10:49899025:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49899026C>A, NC_000011.9:g.49920578C>A, NG_002173.2:g.261G>T, NW_003571045.1:g.57931C>A

Select item 14848928192.

rs1484892819 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:49898716 (GRCh38)
11:49920268 (GRCh37)
Canonical SPDI:: NC_000011.10:49898715:T:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49898716T>A, NC_000011.9:g.49920268T>A, NG_002173.2:g.571A>T, NW_003571045.1:g.57621T>A

Select item 14841148133.

rs1484114813 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:49898803 (GRCh38)
11:49920355 (GRCh37)
Canonical SPDI:: NC_000011.10:49898802:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49898803C>A, NC_000011.9:g.49920355C>A, NG_002173.2:g.484G>T, NW_003571045.1:g.57708C>A

Select item 14754056934.

rs1475405693 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:49899240 (GRCh38)
11:49920792 (GRCh37)
Canonical SPDI:: NC_000011.10:49899239:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000071/10 (GnomAD)
A=0.000076/20 (TOPMED)
HGVS:: NC_000011.10:g.49899240G>A, NC_000011.9:g.49920792G>A, NG_002173.2:g.47C>T, NW_003571045.1:g.58145G>A

Select item 14753541315.

rs1475354131 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:49898470 (GRCh38)
11:49920022 (GRCh37)
Canonical SPDI:: NC_000011.10:49898469:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49898470G>T, NC_000011.9:g.49920022G>T, NG_002173.2:g.817C>A, NW_003571045.1:g.57375G>T

Select item 14679634806.

rs1467963480 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:49899127 (GRCh38)
11:49920679 (GRCh37)
Canonical SPDI:: NC_000011.10:49899126:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49899127A>T, NC_000011.9:g.49920679A>T, NG_002173.2:g.160T>A, NW_003571045.1:g.58032A>T

Select item 14666775257.

rs1466677525 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:49898458 (GRCh38)
11:49920010 (GRCh37)
Canonical SPDI:: NC_000011.10:49898457:G:A,NC_000011.10:49898457:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49898458G>A, NC_000011.10:g.49898458G>T, NC_000011.9:g.49920010G>A, NC_000011.9:g.49920010G>T, NG_002173.2:g.829C>T, NG_002173.2:g.829C>A, NW_003571045.1:g.57363G>A, NW_003571045.1:g.57363G>T

Select item 14642043098.

rs1464204309 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:49898390 (GRCh38)
11:49919942 (GRCh37)
Canonical SPDI:: NC_000011.10:49898389:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000271/38 (GnomAD)
T=0.000272/72 (TOPMED)
HGVS:: NC_000011.10:g.49898390A>T, NC_000011.9:g.49919942A>T, NG_002173.2:g.897T>A, NW_003571045.1:g.57295A>T

Select item 14605581639.

rs1460558163 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 11:49898886 (GRCh38)
11:49920438 (GRCh37)
Canonical SPDI:: NC_000011.10:49898881:TATATA:TATA
Validated:: by frequency,by alfa,by cluster
MAF:: TATA=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.49898882TA[2], NC_000011.9:g.49920434TA[2], NG_002173.2:g.400TA[2], NW_003571045.1:g.57787TA[2]

Select item 146019824710.

rs1460198247 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 11:49899160 (GRCh38)
11:49920712 (GRCh37)
Canonical SPDI:: NC_000011.10:49899159:TT:T
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000068/18 (TOPMED)
HGVS:: NC_000011.10:g.49899161del, NC_000011.9:g.49920713del, NG_002173.2:g.127del, NW_003571045.1:g.58066del

Select item 145931344011.

rs1459313440 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 11:49898485 (GRCh38)
11:49920037 (GRCh37)
Canonical SPDI:: NC_000011.10:49898484:G:A,NC_000011.10:49898484:G:C,NC_000011.10:49898484:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.49898485G>A, NC_000011.10:g.49898485G>C, NC_000011.10:g.49898485G>T, NC_000011.9:g.49920037G>A, NC_000011.9:g.49920037G>C, NC_000011.9:g.49920037G>T, NG_002173.2:g.802C>T, NG_002173.2:g.802C>G, NG_002173.2:g.802C>A, NW_003571045.1:g.57390G>A, NW_003571045.1:g.57390G>C, NW_003571045.1:g.57390G>T

Select item 145225991912.

rs1452259919 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:49898583 (GRCh38)
11:49920135 (GRCh37)
Canonical SPDI:: NC_000011.10:49898582:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.49898583C>T, NC_000011.9:g.49920135C>T, NG_002173.2:g.704G>A, NW_003571045.1:g.57488C>T

Select item 144997755913.

rs1449977559 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:49899214 (GRCh38)
11:49920766 (GRCh37)
Canonical SPDI:: NC_000011.10:49899213:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49899214G>A, NC_000011.9:g.49920766G>A, NG_002173.2:g.73C>T, NW_003571045.1:g.58119G>A

Select item 144924048114.

rs1449240481 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:49898758 (GRCh38)
11:49920310 (GRCh37)
Canonical SPDI:: NC_000011.10:49898757:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49898758C>T, NC_000011.9:g.49920310C>T, NG_002173.2:g.529G>A, NW_003571045.1:g.57663C>T

Select item 144852466015.

rs1448524660 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:49898520 (GRCh38)
11:49920072 (GRCh37)
Canonical SPDI:: NC_000011.10:49898519:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.49898520G>A, NC_000011.9:g.49920072G>A, NG_002173.2:g.767C>T, NW_003571045.1:g.57425G>A

Select item 144698828416.

rs1446988284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:49898411 (GRCh38)
11:49919963 (GRCh37)
Canonical SPDI:: NC_000011.10:49898410:G:A,NC_000011.10:49898410:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000034/9 (TOPMED)
HGVS:: NC_000011.10:g.49898411G>A, NC_000011.10:g.49898411G>T, NC_000011.9:g.49919963G>A, NC_000011.9:g.49919963G>T, NG_002173.2:g.876C>T, NG_002173.2:g.876C>A, NW_003571045.1:g.57316G>A, NW_003571045.1:g.57316G>T

Select item 144678757017.

rs1446787570 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:49899140 (GRCh38)
11:49920692 (GRCh37)
Canonical SPDI:: NC_000011.10:49899139:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49899140G>A, NC_000011.9:g.49920692G>A, NG_002173.2:g.147C>T, NW_003571045.1:g.58045G>A

Select item 144339269718.

rs1443392697 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:49898534 (GRCh38)
11:49920086 (GRCh37)
Canonical SPDI:: NC_000011.10:49898533:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49898534A>G, NC_000011.9:g.49920086A>G, NG_002173.2:g.753T>C, NW_003571045.1:g.57439A>G

Select item 144295839919.

rs1442958399 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:49899259 (GRCh38)
11:49920811 (GRCh37)
Canonical SPDI:: NC_000011.10:49899258:G:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.49899259G>C, NC_000011.9:g.49920811G>C, NG_002173.2:g.28C>G, NW_003571045.1:g.58164G>C

Select item 144105763920.

rs1441057639 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:49898476 (GRCh38)
11:49920028 (GRCh37)
Canonical SPDI:: NC_000011.10:49898475:G:A,NC_000011.10:49898475:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.49898476G>A, NC_000011.10:g.49898476G>T, NC_000011.9:g.49920028G>A, NC_000011.9:g.49920028G>T, NG_002173.2:g.811C>T, NG_002173.2:g.811C>A, NW_003571045.1:g.57381G>A, NW_003571045.1:g.57381G>T

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