SNP Links for Nucleotide (Select 298358766) - SNP

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Links from Nucleotide

Items: 1 to 20 of 216

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Select item 14851513011.

rs1485151301 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176368223 (GRCh38)
1:176337359 (GRCh37)
Canonical SPDI:: NC_000001.11:176368222:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.176368223A>G, NC_000001.10:g.176337359A>G, NG_022744.1:g.513T>C

Select item 14801899452.

rs1480189945 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:176367869 (GRCh38)
1:176337005 (GRCh37)
Canonical SPDI:: NC_000001.11:176367868:T:A,NC_000001.11:176367868:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.176367869T>A, NC_000001.11:g.176367869T>C, NC_000001.10:g.176337005T>A, NC_000001.10:g.176337005T>C, NG_022744.1:g.867A>T, NG_022744.1:g.867A>G

Select item 14741619613.

rs1474161961 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176367995 (GRCh38)
1:176337131 (GRCh37)
Canonical SPDI:: NC_000001.11:176367994:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.176367995A>G, NC_000001.10:g.176337131A>G, NG_022744.1:g.741T>C

Select item 14734975154.

rs1473497515 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:176367868 (GRCh38)
1:176337004 (GRCh37)
Canonical SPDI:: NC_000001.11:176367867:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000312/2 (1000Genomes)
HGVS:: NC_000001.11:g.176367868T>G, NC_000001.10:g.176337004T>G, NG_022744.1:g.868A>C

Select item 14731638495.

rs1473163849 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:176368459 (GRCh38)
1:176337595 (GRCh37)
Canonical SPDI:: NC_000001.11:176368458: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_000001.11:g.176368459C>T, NC_000001.10:g.176337595C>T, NG_022744.1:g.277G>A

Select item 14721330296.

rs1472133029 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:176368088 (GRCh38)
1:176337224 (GRCh37)
Canonical SPDI:: NC_000001.11:176368087:C: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_000001.11:g.176368088C>T, NC_000001.10:g.176337224C>T, NG_022744.1:g.648G>A

Select item 14676922047.

rs1467692204 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:176368610 (GRCh38)
1:176337746 (GRCh37)
Canonical SPDI:: NC_000001.11:176368609:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.176368610T>G, NC_000001.10:g.176337746T>G, NG_022744.1:g.126A>C

Select item 14609940438.

rs1460994043 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:176368555 (GRCh38)
1:176337691 (GRCh37)
Canonical SPDI:: NC_000001.11:176368554:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.176368555T>C, NC_000001.10:g.176337691T>C, NG_022744.1:g.181A>G

Select item 14606359009.

rs1460635900 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:176368699 (GRCh38)
1:176337835 (GRCh37)
Canonical SPDI:: NC_000001.11:176368698:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.176368699T>C, NC_000001.10:g.176337835T>C, NG_022744.1:g.37A>G

Select item 145324296510.

rs1453242965 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176368725 (GRCh38)
1:176337861 (GRCh37)
Canonical SPDI:: NC_000001.11:176368724:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.176368725A>G, NC_000001.10:g.176337861A>G, NG_022744.1:g.11T>C

Select item 145222665911.

rs1452226659 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:176368039 (GRCh38)
1:176337175 (GRCh37)
Canonical SPDI:: NC_000001.11:176368038:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.176368039T>C, NC_000001.10:g.176337175T>C, NG_022744.1:g.697A>G

Select item 145138778712.

rs1451387787 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176368206 (GRCh38)
1:176337342 (GRCh37)
Canonical SPDI:: NC_000001.11:176368205:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.176368206A>G, NC_000001.10:g.176337342A>G, NG_022744.1:g.530T>C

Select item 144856920613.

rs1448569206 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:176367622 (GRCh38)
1:176336758 (GRCh37)
Canonical SPDI:: NC_000001.11:176367621:C:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.176367622C>G, NC_000001.10:g.176336758C>G, NG_022744.1:g.1114G>C

Select item 144404122614.

rs1444041226 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:176367724 (GRCh38)
1:176336860 (GRCh37)
Canonical SPDI:: NC_000001.11:176367723:C:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.176367724C>A, NC_000001.10:g.176336860C>A, NG_022744.1:g.1012G>T

Select item 144025106015.

rs1440251060 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:176368668 (GRCh38)
1:176337804 (GRCh37)
Canonical SPDI:: NC_000001.11:176368667:C:G,NC_000001.11:176368667:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.176368668C>G, NC_000001.11:g.176368668C>T, NC_000001.10:g.176337804C>G, NC_000001.10:g.176337804C>T, NG_022744.1:g.68G>C, NG_022744.1:g.68G>A

Select item 143806906416.

rs1438069064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176368155 (GRCh38)
1:176337291 (GRCh37)
Canonical SPDI:: NC_000001.11:176368154:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.176368155A>G, NC_000001.10:g.176337291A>G, NG_022744.1:g.581T>C

Select item 142864241217.

rs1428642412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:176368590 (GRCh38)
1:176337726 (GRCh37)
Canonical SPDI:: NC_000001.11:176368589:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.176368590A>G, NC_000001.10:g.176337726A>G, NG_022744.1:g.146T>C

Select item 142681528318.

rs1426815283 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:176368308 (GRCh38)
1:176337444 (GRCh37)
Canonical SPDI:: NC_000001.11:176368307:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.176368308T>C, NC_000001.10:g.176337444T>C, NG_022744.1:g.428A>G

Select item 142563093319.

rs1425630933 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACTGTGGGGTCCA>- [Show Flanks]
Chromosome:: 1:176368223 (GRCh38)
1:176337359 (GRCh37)
Canonical SPDI:: NC_000001.11:176368220:CAACTGTGGGGTCCA:CA
Validated:: by frequency,by alfa
MAF:: CA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.176368223_176368235del, NC_000001.10:g.176337359_176337371del, NG_022744.1:g.503_515del

Select item 141813353020.

rs1418133530 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:176368135 (GRCh38)
1:176337271 (GRCh37)
Canonical SPDI:: NC_000001.11:176368134:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000001.11:g.176368135A>T, NC_000001.10:g.176337271A>T, NG_022744.1:g.601T>A