SNP Links for Gene (Select 29989) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14908858561.

rs1490885856 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:133214761 (GRCh38)
9:136090148 (GRCh37)
Canonical SPDI:: NC_000009.12:133214760:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.133214761C>T, NC_000009.11:g.136090148C>T, NW_009646201.1:g.40707C>T, NW_003315925.1:g.40707C>T

Select item 14906614872.

rs1490661487 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:133213882 (GRCh38)
9:136089269 (GRCh37)
Canonical SPDI:: NC_000009.12:133213881:C:A,NC_000009.12:133213881:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00011/2 (TOMMO)
T=0.00274/8 (KOREAN)
HGVS:: NC_000009.12:g.133213882C>A, NC_000009.12:g.133213882C>T, NC_000009.11:g.136089269C>A, NC_000009.11:g.136089269C>T, NW_009646201.1:g.39828C>A, NW_009646201.1:g.39828C>T, NW_003315925.1:g.39828C>A, NW_003315925.1:g.39828C>T

Select item 14906554543.

rs1490655454 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:133208331 (GRCh38)
9:136083718 (GRCh37)
Canonical SPDI:: NC_000009.12:133208330:G:A
Gene:: OBP2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.133208331G>A, NC_000009.11:g.136083718G>A, NW_009646201.1:g.34277G>A, NW_003315925.1:g.34277G>A

Select item 14906146514.

rs1490614651 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:133217057 (GRCh38)
9:136092444 (GRCh37)
Canonical SPDI:: NC_000009.12:133217056:C:G
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133217057C>G, NC_000009.11:g.136092444C>G, NW_009646201.1:g.43003C>G, NW_003315925.1:g.43003C>G

Select item 14903310875.

rs1490331087 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:133210740 (GRCh38)
9:136086127 (GRCh37)
Canonical SPDI:: NC_000009.12:133210739:T:C
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000035/1 (TOMMO)
HGVS:: NC_000009.12:g.133210740T>C, NC_000009.11:g.136086127T>C, NW_009646201.1:g.36686T>C, NW_003315925.1:g.36686T>C

Select item 14903180406.

rs1490318040 has merged into rs115038053 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:133208381 (GRCh38)
9:136083768 (GRCh37)
Canonical SPDI:: NC_000009.12:133208380:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.025728/486 (ALFA)
T=0.014981/8 (MGP)
T=0.044191/221 (1000Genomes)
T=0.044768/6276 (GnomAD)
T=0.047512/12576 (TOPMED)
T=0.055556/12 (Qatari)
C=0.40625/13 (SGDP_PRJ)
HGVS:: NC_000009.12:g.133208381C>T, NC_000009.11:g.136083768C>T, NW_009646201.1:g.34327C>T, NW_003315925.1:g.34327C>T

Select item 14897919157.

rs1489791915 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:133215775 (GRCh38)
9:136091162 (GRCh37)
Canonical SPDI:: NC_000009.12:133215774:C:G
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000498/7 (ALFA)
G=0.000613/86 (GnomAD)
G=0.00062/164 (TOPMED)
HGVS:: NC_000009.12:g.133215775C>G, NC_000009.11:g.136091162C>G, NW_009646201.1:g.41721C>G, NW_003315925.1:g.41721C>G

Select item 14896432178.

rs1489643217 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:133224258 (GRCh38)
9:136099645 (GRCh37)
Canonical SPDI:: NC_000009.12:133224257:G:T
Gene:: OBP2B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000009.12:g.133224258G>T, NC_000009.11:g.136099645G>T, NW_009646201.1:g.50204G>T, NW_003315925.1:g.50204G>T

Select item 14895994319.

rs1489599431 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:133218556 (GRCh38)
9:136093943 (GRCh37)
Canonical SPDI:: NC_000009.12:133218555:A:T
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.133218556A>T, NC_000009.11:g.136093943A>T, NW_009646201.1:g.44502A>T, NW_003315925.1:g.44502A>T

Select item 148936180410.

rs1489361804 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:133217061 (GRCh38)
9:136092448 (GRCh37)
Canonical SPDI:: NC_000009.12:133217060:C:G
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_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_000009.12:g.133217061C>G, NC_000009.11:g.136092448C>G, NW_009646201.1:g.43007C>G, NW_003315925.1:g.43007C>G

Select item 148923595011.

rs1489235950 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:133209826 (GRCh38)
9:136085213 (GRCh37)
Canonical SPDI:: NC_000009.12:133209825:T:G
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.133209826T>G, NC_000009.11:g.136085213T>G, NW_009646201.1:g.35772T>G, NW_003315925.1:g.35772T>G

Select item 148920487812.

rs1489204878 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:133207113 (GRCh38)
9:136082500 (GRCh37)
Canonical SPDI:: NC_000009.12:133207112:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.133207113C>T, NC_000009.11:g.136082500C>T, NW_009646201.1:g.33059C>T, NW_003315925.1:g.33059C>T

Select item 148908330813.

rs1489083308 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:133222101 (GRCh38)
9:136097488 (GRCh37)
Canonical SPDI:: NC_000009.12:133222100:G:A,NC_000009.12:133222100:G:T
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.133222101G>A, NC_000009.12:g.133222101G>T, NC_000009.11:g.136097488G>A, NC_000009.11:g.136097488G>T, NW_009646201.1:g.48047G>A, NW_009646201.1:g.48047G>T, NW_003315925.1:g.48047G>A, NW_003315925.1:g.48047G>T

Select item 148897118914.

rs1488971189 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:133221107 (GRCh38)
9:136096494 (GRCh37)
Canonical SPDI:: NC_000009.12:133221106:G:A
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133221107G>A, NC_000009.11:g.136096494G>A, NW_009646201.1:g.47053G>A, NW_003315925.1:g.47053G>A

Select item 148897005415.

rs1488970054 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 9:133207390 (GRCh38)
9:136082777 (GRCh37)
Canonical SPDI:: NC_000009.12:133207389:T:C,NC_000009.12:133207389:T:G
Gene:: OBP2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.133207390T>C, NC_000009.12:g.133207390T>G, NC_000009.11:g.136082777T>C, NC_000009.11:g.136082777T>G, NW_009646201.1:g.33336T>C, NW_009646201.1:g.33336T>G, NW_003315925.1:g.33336T>C, NW_003315925.1:g.33336T>G

Select item 148896210916.

rs1488962109 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 9:133208311 (GRCh38)
9:136083698 (GRCh37)
Canonical SPDI:: NC_000009.12:133208310:C:A,NC_000009.12:133208310:C:G,NC_000009.12:133208310:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.133208311C>A, NC_000009.12:g.133208311C>G, NC_000009.12:g.133208311C>T, NC_000009.11:g.136083698C>A, NC_000009.11:g.136083698C>G, NC_000009.11:g.136083698C>T, NW_009646201.1:g.34257C>A, NW_009646201.1:g.34257C>G, NW_009646201.1:g.34257C>T, NW_003315925.1:g.34257C>A, NW_003315925.1:g.34257C>G, NW_003315925.1:g.34257C>T

Select item 148896197917.

rs1488961979 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:133224553 (GRCh38)
9:136099940 (GRCh37)
Canonical SPDI:: NC_000009.12:133224552:G:A,NC_000009.12:133224552:G:T
Gene:: OBP2B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000009.12:g.133224553G>A, NC_000009.12:g.133224553G>T, NC_000009.11:g.136099940G>A, NC_000009.11:g.136099940G>T, NW_009646201.1:g.50499G>A, NW_009646201.1:g.50499G>T, NW_003315925.1:g.50499G>A, NW_003315925.1:g.50499G>T

Select item 148895590318.

rs1488955903 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:133212107 (GRCh38)
9:136087494 (GRCh37)
Canonical SPDI:: NC_000009.12:133212106:A:G
Gene:: OBP2B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_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_000009.12:g.133212107A>G, NC_000009.11:g.136087494A>G, NW_009646201.1:g.38053A>G, NW_003315925.1:g.38053A>G

Select item 148892207719.

rs1488922077 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:133209917 (GRCh38)
9:136085304 (GRCh37)
Canonical SPDI:: NC_000009.12:133209916:C:T
Gene:: OBP2B (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133209917C>T, NC_000009.11:g.136085304C>T, NW_009646201.1:g.35863C>T, NW_003315925.1:g.35863C>T, XM_017014654.2:c.-51G>A, XM_017014654.1:c.-51G>A, XM_047423295.1:c.-51G>A