SNP Links for Gene (Select 442900) - SNP

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Links from Gene

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Select item 14904307691.

rs1490430769 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75337049 (GRCh38)
11:75048093 (GRCh37)
Canonical SPDI:: NC_000011.10:75337048:T:C
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_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_000011.10:g.75337049T>C, NC_000011.9:g.75048093T>C, NG_028118.1:g.19783A>G

Select item 14862010892.

rs1486201089 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:75334931 (GRCh38)
11:75045975 (GRCh37)
Canonical SPDI:: NC_000011.10:75334930:T:C,NC_000011.10:75334930:T:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
C=0.000035/1 (TOMMO)
G=0.0002/3 (GnomAD)
HGVS:: NC_000011.10:g.75334931T>C, NC_000011.10:g.75334931T>G, NC_000011.9:g.75045975T>C, NC_000011.9:g.75045975T>G, NG_028118.1:g.21901A>G, NG_028118.1:g.21901A>C

Select item 14857957953.

rs1485795795 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75335504 (GRCh38)
11:75046548 (GRCh37)
Canonical SPDI:: NC_000011.10:75335503:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.75335504G>A, NC_000011.9:g.75046548G>A, NG_028118.1:g.21328C>T

Select item 14817981804.

rs1481798180 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:75336403 (GRCh38)
11:75047447 (GRCh37)
Canonical SPDI:: NC_000011.10:75336402:C:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.75336403C>A, NC_000011.9:g.75047447C>A, NG_028118.1:g.20429G>T

Select item 14800349475.

rs1480034947 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335318 (GRCh38)
11:75046362 (GRCh37)
Canonical SPDI:: NC_000011.10:75335317:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.75335318C>T, NC_000011.9:g.75046362C>T, NG_028118.1:g.21514G>A

Select item 14800038126.

rs1480003812 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75336302 (GRCh38)
11:75047346 (GRCh37)
Canonical SPDI:: NC_000011.10:75336301:T:C
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_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_000011.10:g.75336302T>C, NC_000011.9:g.75047346T>C, NG_028118.1:g.20530A>G

Select item 14796784947.

rs1479678494 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75336746 (GRCh38)
11:75047790 (GRCh37)
Canonical SPDI:: NC_000011.10:75336745:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75336746G>A, NC_000011.9:g.75047790G>A, NG_028118.1:g.20086C>T

Select item 14738322348.

rs1473832234 has merged into rs11284367 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TTTT,TTTTTT [Show Flanks]
Chromosome:: 11:75334935 (GRCh38)
11:75045979 (GRCh37)
Canonical SPDI:: NC_000011.10:75334929:TTTTTTTTTT:TTTTT,NC_000011.10:75334929:TTTTTTTTTT:TTTTTTTTT,NC_000011.10:75334929:TTTTTTTTTT:TTTTTTTTTTT
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0.312022/82589 (TOPMED)
T=0.322276/1195 (TWINSUK)
T=0.329528/1270 (ALSPAC)
T=0.343687/343 (GoNL)
T=0.35024/1754 (1000Genomes)
T=0.45/18 (GENOME_DK)
-=0.494536/905 (Korea1K)
HGVS:: NC_000011.10:g.75334935_75334939del, NC_000011.10:g.75334939del, NC_000011.10:g.75334939dup, NC_000011.9:g.75045979_75045983del, NC_000011.9:g.75045983del, NC_000011.9:g.75045983dup, NG_028118.1:g.21898_21902del, NG_028118.1:g.21902del, NG_028118.1:g.21902dup

Select item 14737996699.

rs1473799669 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335854 (GRCh38)
11:75046898 (GRCh37)
Canonical SPDI:: NC_000011.10:75335853:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_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_000011.10:g.75335854C>T, NC_000011.9:g.75046898C>T, NG_028118.1:g.20978G>A

Select item 147360153210.

rs1473601532 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335022 (GRCh38)
11:75046066 (GRCh37)
Canonical SPDI:: NC_000011.10:75335021:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75335022A>G, NC_000011.9:g.75046066A>G, NG_028118.1:g.21810T>C

Select item 147151048211.

rs1471510482 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335406 (GRCh38)
11:75046450 (GRCh37)
Canonical SPDI:: NC_000011.10:75335405:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75335406A>G, NC_000011.9:g.75046450A>G, NG_028118.1:g.21426T>C

Select item 146917283512.

rs1469172835 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75336427 (GRCh38)
11:75047471 (GRCh37)
Canonical SPDI:: NC_000011.10:75336426:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_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_000011.10:g.75336427C>T, NC_000011.9:g.75047471C>T, NG_028118.1:g.20405G>A

Select item 146864606613.

rs1468646066 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75336838 (GRCh38)
11:75047882 (GRCh37)
Canonical SPDI:: NC_000011.10:75336837:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.75336838A>G, NC_000011.9:g.75047882A>G, NG_028118.1:g.19994T>C

Select item 146787300514.

rs1467873005 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75336527 (GRCh38)
11:75047571 (GRCh37)
Canonical SPDI:: NC_000011.10:75336526:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75336527C>T, NC_000011.9:g.75047571C>T, NG_028118.1:g.20305G>A

Select item 146614616315.

rs1466146163 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:75335990 (GRCh38)
11:75047034 (GRCh37)
Canonical SPDI:: NC_000011.10:75335989:A:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_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_000011.10:g.75335990A>T, NC_000011.9:g.75047034A>T, NG_028118.1:g.20842T>A

Select item 146194813516.

rs1461948135 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:75337001 (GRCh38)
11:75048045 (GRCh37)
Canonical SPDI:: NC_000011.10:75337000:T:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00007/1 (ALFA)
HGVS:: NC_000011.10:g.75337001T>A, NC_000011.9:g.75048045T>A, NG_028118.1:g.19831A>T

Select item 145997463217.

rs1459974632 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75336890 (GRCh38)
11:75047934 (GRCh37)
Canonical SPDI:: NC_000011.10:75336889:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.75336890G>A, NC_000011.9:g.75047934G>A, NG_028118.1:g.19942C>T

Select item 145934654018.

rs1459346540 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75334605 (GRCh38)
11:75045649 (GRCh37)
Canonical SPDI:: NC_000011.10:75334604:T:C
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,500B_downstream_variant,intron_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.75334605T>C, NC_000011.9:g.75045649T>C, NG_028118.1:g.22227A>G

Select item 145929386219.

rs1459293862 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75335585 (GRCh38)
11:75046629 (GRCh37)
Canonical SPDI:: NC_000011.10:75335584:T:C
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75335585T>C, NC_000011.9:g.75046629T>C, NG_028118.1:g.21247A>G

Select item 145924165020.

rs1459241650 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75335961 (GRCh38)
11:75047005 (GRCh37)
Canonical SPDI:: NC_000011.10:75335960:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_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_000011.10:g.75335961G>A, NC_000011.9:g.75047005G>A, NG_028118.1:g.20871C>T

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