SNP Links for Gene (Select 100126304) - SNP

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Select item 14909693851.

rs1490969385 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:146002212 (GRCh38)
X:145083730 (GRCh37)
Canonical SPDI:: NC_000023.11:146002211:T:A
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/2 (GnomAD)
A=0.000049/13 (TOPMED)
HGVS:: NC_000023.11:g.146002212T>A, NC_000023.10:g.145083730T>A, NW_004070890.2:g.1526603T>A

Select item 14877069502.

rs1487706950 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:146002103 (GRCh38)
X:145083621 (GRCh37)
Canonical SPDI:: NC_000023.11:146002102:C:A
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000038/4 (GnomAD)
A=0.000072/19 (TOPMED)
HGVS:: NC_000023.11:g.146002103C>A, NC_000023.10:g.145083621C>A, NW_004070890.2:g.1526494C>A

Select item 14857400513.

rs1485740051 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: X:146003108 (GRCh38)
X:145084626 (GRCh37)
Canonical SPDI:: NC_000023.11:146003107:AT:
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.146003108_146003109del, NC_000023.10:g.145084626_145084627del, NW_004070890.2:g.1527499_1527500del

Select item 14836405514.

rs1483640551 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:146001257 (GRCh38)
X:145082775 (GRCh37)
Canonical SPDI:: NC_000023.11:146001256:T:C
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000023/6 (TOPMED)
C=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.146001257T>C, NC_000023.10:g.145082775T>C, NW_004070890.2:g.1525648T>C

Select item 14816648035.

rs1481664803 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:146001824 (GRCh38)
X:145083342 (GRCh37)
Canonical SPDI:: NC_000023.11:146001823:T:A
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.146001824T>A, NC_000023.10:g.145083342T>A, NW_004070890.2:g.1526215T>A

Select item 14816324516.

rs1481632451 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146001236 (GRCh38)
X:145082754 (GRCh37)
Canonical SPDI:: NC_000023.11:146001235:A:G
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.146001236A>G, NC_000023.10:g.145082754A>G, NW_004070890.2:g.1525627A>G

Select item 14796995837.

rs1479699583 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:146002823 (GRCh38)
X:145084341 (GRCh37)
Canonical SPDI:: NC_000023.11:146002822:C:T
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.146002823C>T, NC_000023.10:g.145084341C>T, NW_004070890.2:g.1527214C>T

Select item 14756225568.

rs1475622556 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:146002724 (GRCh38)
X:145084242 (GRCh37)
Canonical SPDI:: NC_000023.11:146002723:C:A,NC_000023.11:146002723:C:T
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00006/1 (ALFA)
T=0.00004/4 (GnomAD)
T=0.00021/1 (1000Genomes)
T=0.00036/5 (TOMMO)
HGVS:: NC_000023.11:g.146002724C>A, NC_000023.11:g.146002724C>T, NC_000023.10:g.145084242C>A, NC_000023.10:g.145084242C>T, NW_004070890.2:g.1527115C>A, NW_004070890.2:g.1527115C>T

Select item 14755119939.

rs1475511993 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146001592 (GRCh38)
X:145083110 (GRCh37)
Canonical SPDI:: NC_000023.11:146001591:A:G
Gene:: MIR891B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.146001592A>G, NC_000023.10:g.145083110A>G, NW_004070890.2:g.1525983A>G

Select item 147310570710.

rs1473105707 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:146001359 (GRCh38)
X:145082877 (GRCh37)
Canonical SPDI:: NC_000023.11:146001358:T:C
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000023/6 (TOPMED)
C=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.146001359T>C, NC_000023.10:g.145082877T>C, NW_004070890.2:g.1525750T>C

Select item 147273389211.

rs1472733892 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:146001457 (GRCh38)
X:145082975 (GRCh37)
Canonical SPDI:: NC_000023.11:146001456:C:T
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.146001457C>T, NC_000023.10:g.145082975C>T, NW_004070890.2:g.1525848C>T

Select item 147147027412.

rs1471470274 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146001794 (GRCh38)
X:145083312 (GRCh37)
Canonical SPDI:: NC_000023.11:146001793:A:G
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000324/6 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.146001794A>G, NC_000023.10:g.145083312A>G, NW_004070890.2:g.1526185A>G

Select item 147119634613.

rs1471196346 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAATT>- [Show Flanks]
Chromosome:: X:146002978 (GRCh38)
X:145084496 (GRCh37)
Canonical SPDI:: NC_000023.11:146002973:AATTTAATT:AATT
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AATT=0.000214/3 (ALFA)
-=0.000091/24 (TOPMED)
-=0.000097/10 (GnomAD)
HGVS:: NC_000023.11:g.146002978_146002982del, NC_000023.10:g.145084496_145084500del, NW_004070890.2:g.1527369_1527373del

Select item 147116907814.

rs1471169078 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:146002454 (GRCh38)
X:145083972 (GRCh37)
Canonical SPDI:: NC_000023.11:146002453:G:T
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.00014/2 (ALFA)
HGVS:: NC_000023.11:g.146002454G>T, NC_000023.10:g.145083972G>T, NW_004070890.2:g.1526845G>T

Select item 147105838815.

rs1471058388 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:146001337 (GRCh38)
X:145082855 (GRCh37)
Canonical SPDI:: NC_000023.11:146001336:G:T
Gene:: MIR891B (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=0.00001/1 (GnomAD)
T=0.00036/5 (TOMMO)
T=0.001027/3 (KOREAN)
HGVS:: NC_000023.11:g.146001337G>T, NC_000023.10:g.145082855G>T, NW_004070890.2:g.1525728G>T

Select item 146892838816.

rs1468928388 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:146001786 (GRCh38)
X:145083304 (GRCh37)
Canonical SPDI:: NC_000023.11:146001785:C:G
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0.000142/2 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.146001786C>G, NC_000023.10:g.145083304C>G, NW_004070890.2:g.1526177C>G

Select item 146516493817.

rs1465164938 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:146000721 (GRCh38)
X:145082239 (GRCh37)
Canonical SPDI:: NC_000023.11:146000720:A:C
Gene:: MIR891B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.146000721A>C, NC_000023.10:g.145082239A>C, NW_004070890.2:g.1525112A>C

Select item 146469732718.

rs1464697327 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:146002301 (GRCh38)
X:145083819 (GRCh37)
Canonical SPDI:: NC_000023.11:146002300:A:C
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.146002301A>C, NC_000023.10:g.145083819A>C, NW_004070890.2:g.1526692A>C

Select item 146447589919.

rs1464475899 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146000959 (GRCh38)
X:145082477 (GRCh37)
Canonical SPDI:: NC_000023.11:146000958:A:G
Gene:: MIR891B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.146000959A>G, NC_000023.10:g.145082477A>G, NW_004070890.2:g.1525350A>G

Select item 146197605120.

rs1461976051 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146001827 (GRCh38)
X:145083345 (GRCh37)
Canonical SPDI:: NC_000023.11:146001826:A:G
Gene:: MIR891B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.146001827A>G, NC_000023.10:g.145083345A>G, NW_004070890.2:g.1526218A>G

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