SNP Links for Nucleotide (Select 962611251) - SNP

Links from Nucleotide

Items: 1 to 20 of 476

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Select item 14868700241.

rs1486870024 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:73195587 (GRCh38)
5:72491414 (GRCh37)
Canonical SPDI:: NC_000005.10:73195586:T:C
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000005.10:g.73195587T>C, NC_000005.9:g.72491414T>C, NR_134291.1:n.2062A>G

Select item 14831191482.

rs1483119148 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:73196864 (GRCh38)
5:72492691 (GRCh37)
Canonical SPDI:: NC_000005.10:73196863:G:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73196864G>A, NC_000005.9:g.72492691G>A, NR_134291.1:n.785C>T

Select item 14829634993.

rs1482963499 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:73196434 (GRCh38)
5:72492261 (GRCh37)
Canonical SPDI:: NC_000005.10:73196433:C:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000005.10:g.73196434C>A, NC_000005.9:g.72492261C>A, NR_134291.1:n.1215G>T

Select item 14813806954.

rs1481380695 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:73196263 (GRCh38)
5:72492090 (GRCh37)
Canonical SPDI:: NC_000005.10:73196262:C:T
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.73196263C>T, NC_000005.9:g.72492090C>T, NR_134291.1:n.1386G>A

Select item 14807940275.

rs1480794027 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:73199167 (GRCh38)
5:72494994 (GRCh37)
Canonical SPDI:: NC_000005.10:73199166:G:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.73199167G>A, NC_000005.9:g.72494994G>A, NR_134291.1:n.237C>T

Select item 14785889766.

rs1478588976 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:73196123 (GRCh38)
5:72491950 (GRCh37)
Canonical SPDI:: NC_000005.10:73196122:C:T
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.73196123C>T, NC_000005.9:g.72491950C>T, NR_134291.1:n.1526G>A

Select item 14776729277.

rs1477672927 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:73195836 (GRCh38)
5:72491663 (GRCh37)
Canonical SPDI:: NC_000005.10:73195835:A:G
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73195836A>G, NC_000005.9:g.72491663A>G, NR_134291.1:n.1813T>C

Select item 14759972298.

rs1475997229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:73195919 (GRCh38)
5:72491746 (GRCh37)
Canonical SPDI:: NC_000005.10:73195918:T:C
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73195919T>C, NC_000005.9:g.72491746T>C, NR_134291.1:n.1730A>G

Select item 14750679959.

rs1475067995 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:73195966 (GRCh38)
5:72491793 (GRCh37)
Canonical SPDI:: NC_000005.10:73195965:A:G
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000045/12 (TOPMED)
G=0.000071/10 (GnomAD)
HGVS:: NC_000005.10:g.73195966A>G, NC_000005.9:g.72491793A>G, NR_134291.1:n.1683T>C

Select item 147185290210.

rs1471852902 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:73197326 (GRCh38)
5:72493153 (GRCh37)
Canonical SPDI:: NC_000005.10:73197325:G:C
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73197326G>C, NC_000005.9:g.72493153G>C, NR_134291.1:n.323C>G

Select item 147155412311.

rs1471554123 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 5:73196021 (GRCh38)
5:72491848 (GRCh37)
Canonical SPDI:: NC_000005.10:73196020:T:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000005.10:g.73196021T>A, NC_000005.9:g.72491848T>A, NR_134291.1:n.1628A>T

Select item 146772505912.

rs1467725059 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:73201825 (GRCh38)
5:72497652 (GRCh37)
Canonical SPDI:: NC_000005.10:73201824:C:T
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000005.10:g.73201825C>T, NC_000005.9:g.72497652C>T, NR_134291.1:n.137G>A

Select item 146620943513.

rs1466209435 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 5:73196543 (GRCh38)
5:72492370 (GRCh37)
Canonical SPDI:: NC_000005.10:73196542:T:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.73196543T>A, NC_000005.9:g.72492370T>A, NR_134291.1:n.1106A>T

Select item 146540052314.

rs1465400523 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:73196993 (GRCh38)
5:72492820 (GRCh37)
Canonical SPDI:: NC_000005.10:73196992:G:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.73196993G>A, NC_000005.9:g.72492820G>A, NR_134291.1:n.656C>T

Select item 146485608915.

rs1464856089 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:73196043 (GRCh38)
5:72491870 (GRCh37)
Canonical SPDI:: NC_000005.10:73196042:G:C
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000005.10:g.73196043G>C, NC_000005.9:g.72491870G>C, NR_134291.1:n.1606C>G

Select item 146351076616.

rs1463510766 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:73195524 (GRCh38)
5:72491351 (GRCh37)
Canonical SPDI:: NC_000005.10:73195523:G:T
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73195524G>T, NC_000005.9:g.72491351G>T, NR_134291.1:n.2125C>A

Select item 146336839317.

rs1463368393 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 5:73196559 (GRCh38)
5:72492386 (GRCh37)
Canonical SPDI:: NC_000005.10:73196558:C:A,NC_000005.10:73196558:C:T
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73196559C>A, NC_000005.10:g.73196559C>T, NC_000005.9:g.72492386C>A, NC_000005.9:g.72492386C>T, NR_134291.1:n.1090G>T, NR_134291.1:n.1090G>A

Select item 146308712318.

rs1463087123 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:73196937 (GRCh38)
5:72492764 (GRCh37)
Canonical SPDI:: NC_000005.10:73196936:G:A
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.73196937G>A, NC_000005.9:g.72492764G>A, NR_134291.1:n.712C>T

Select item 146271733319.

rs1462717333 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:73195639 (GRCh38)
5:72491466 (GRCh37)
Canonical SPDI:: NC_000005.10:73195638:T:C
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.73195639T>C, NC_000005.9:g.72491466T>C, NR_134291.1:n.2010A>G

Select item 146119848720.

rs1461198487 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 5:73195508 (GRCh38)
5:72491335 (GRCh37)
Canonical SPDI:: NC_000005.10:73195507:T:C,NC_000005.10:73195507:T:G
Gene:: LOC340090 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.73195508T>C, NC_000005.10:g.73195508T>G, NC_000005.9:g.72491335T>C, NC_000005.9:g.72491335T>G, NR_134291.1:n.2141A>G, NR_134291.1:n.2141A>C

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