SNP Links for Gene (Select 100302212) - SNP

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Select item 14914960401.

rs1491496040 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 3:75631081 (GRCh38)
3:75680232 (GRCh37)
Canonical SPDI:: NC_000003.12:75631078:TATA:TA
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
HGVS:: NC_000003.12:g.75631079TA[1], NC_000003.11:g.75680230TA[1], NG_046708.1:g.1188TA[1]

Select item 14887056702.

rs1488705670 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:75631046 (GRCh38)
3:75680197 (GRCh37)
Canonical SPDI:: NC_000003.12:75631045:G:A
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000003.12:g.75631046G>A, NC_000003.11:g.75680197G>A, NG_046708.1:g.1155G>A

Select item 14875382913.

rs1487538291 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:75630879 (GRCh38)
3:75680030 (GRCh37)
Canonical SPDI:: NC_000003.12:75630878:A:C
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.75630879A>C, NC_000003.11:g.75680030A>C, NG_046708.1:g.988A>C

Select item 14865151884.

rs1486515188 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:75629665 (GRCh38)
3:75678816 (GRCh37)
Canonical SPDI:: NC_000003.12:75629664:A:G
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000057/8 (GnomAD)
G=0.000083/22 (TOPMED)
HGVS:: NC_000003.12:g.75629665A>G, NC_000003.11:g.75678816A>G

Select item 14858495365.

rs1485849536 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 3:75628895 (GRCh38)
3:75678046 (GRCh37)
Canonical SPDI:: NC_000003.12:75628894:A:C,NC_000003.12:75628894:A:G
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.03812/435 (ALFA)
G=0.07881/2227 (TOMMO)
G=0.13997/409 (KOREAN)
HGVS:: NC_000003.12:g.75628895A>C, NC_000003.12:g.75628895A>G, NC_000003.11:g.75678046A>C, NC_000003.11:g.75678046A>G

Select item 14851755516.

rs1485175551 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 3:75629373 (GRCh38)
3:75678524 (GRCh37)
Canonical SPDI:: NC_000003.12:75629372:G:C,NC_000003.12:75629372:G:T
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.75629373G>C, NC_000003.12:g.75629373G>T, NC_000003.11:g.75678524G>C, NC_000003.11:g.75678524G>T

Select item 14847501317.

rs1484750131 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:75628903 (GRCh38)
3:75678054 (GRCh37)
Canonical SPDI:: NC_000003.12:75628902:C:A
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00438/52 (ALFA)
A=0.06468/189 (KOREAN)
A=0.06724/1900 (TOMMO)
HGVS:: NC_000003.12:g.75628903C>A, NC_000003.11:g.75678054C>A

Select item 14840933138.

rs1484093313 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:75630597 (GRCh38)
3:75679748 (GRCh37)
Canonical SPDI:: NC_000003.12:75630596:A:G
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000036/5 (GnomAD)
HGVS:: NC_000003.12:g.75630597A>G, NC_000003.11:g.75679748A>G, NG_046708.1:g.706A>G

Select item 14840644559.

rs1484064455 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>A
Chromosome:: no mapping
Canonical SPDI:

Select item 148365581110.

rs1483655811 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>A
Chromosome:: no mapping
Canonical SPDI:

Select item 148358705711.

rs1483587057 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:75630984 (GRCh38)
3:75680135 (GRCh37)
Canonical SPDI:: NC_000003.12:75630983:C:T
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.075312/1230 (ALFA)
T=0.007871/23 (KOREAN)
T=0.054612/5991 (GnomAD)
T=0.070635/1996 (TOMMO)
T=0.078857/505 (1000Genomes)
HGVS:: NC_000003.12:g.75630984C>T, NC_000003.11:g.75680135C>T, NG_046708.1:g.1093C>T

Select item 148331103912.

rs1483311039 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:75629276 (GRCh38)
3:75678427 (GRCh37)
Canonical SPDI:: NC_000003.12:75629275:A:G
Gene:: MIR1324 (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_000003.12:g.75629276A>G, NC_000003.11:g.75678427A>G

Select item 148085242013.

rs1480852420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:75630677 (GRCh38)
3:75679828 (GRCh37)
Canonical SPDI:: NC_000003.12:75630676:C:A
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000531/5 (TOMMO)
A=0.001092/2 (Korea1K)
HGVS:: NC_000003.12:g.75630677C>A, NC_000003.11:g.75679828C>A, NG_046708.1:g.786C>A

Select item 148082293714.

rs1480822937 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:75629873 (GRCh38)
3:75679024 (GRCh37)
Canonical SPDI:: NC_000003.12:75629872:C:T
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000034/9 (TOPMED)
T=0.041752/122 (KOREAN)
HGVS:: NC_000003.12:g.75629873C>T, NC_000003.11:g.75679024C>T

Select item 148017778215.

rs1480177782 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:75629090 (GRCh38)
3:75678241 (GRCh37)
Canonical SPDI:: NC_000003.12:75629089:T:C
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.75629090T>C, NC_000003.11:g.75678241T>C

Select item 148003775516.

rs1480037755 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:75631178 (GRCh38)
3:75680329 (GRCh37)
Canonical SPDI:: NC_000003.12:75631177:C:A,NC_000003.12:75631177:C:T
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.75631178C>A, NC_000003.12:g.75631178C>T, NC_000003.11:g.75680329C>A, NC_000003.11:g.75680329C>T, NG_046708.1:g.1287C>A, NG_046708.1:g.1287C>T

Select item 147996957817.

rs1479969578 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:75630370 (GRCh38)
3:75679521 (GRCh37)
Canonical SPDI:: NC_000003.12:75630369:G:A,NC_000003.12:75630369:G:C
Gene:: MIR1324 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00203/13 (1000Genomes)
HGVS:: NC_000003.12:g.75630370G>A, NC_000003.12:g.75630370G>C, NC_000003.11:g.75679521G>A, NC_000003.11:g.75679521G>C, NG_046708.1:g.479G>A, NG_046708.1:g.479G>C

Select item 147902883318.

rs1479028833 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:75631039 (GRCh38)
3:75680190 (GRCh37)
Canonical SPDI:: NC_000003.12:75631038:C:G,NC_000003.12:75631038:C:T
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000106/3 (TOMMO)
T=0.000937/6 (1000Genomes)
HGVS:: NC_000003.12:g.75631039C>G, NC_000003.12:g.75631039C>T, NC_000003.11:g.75680190C>G, NC_000003.11:g.75680190C>T, NG_046708.1:g.1148C>G, NG_046708.1:g.1148C>T

Select item 147856348719.

rs1478563487 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 3:75631321 (GRCh38)
3:75680472 (GRCh37)
Canonical SPDI:: NC_000003.12:75631320:GG:G
Gene:: MIR1324 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.00109/7 (1000Genomes)
HGVS:: NC_000003.12:g.75631322del, NC_000003.11:g.75680473del, NG_046708.1:g.1431del

Select item 147827005920.

rs1478270059 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>C
Chromosome:: no mapping
Canonical SPDI:

dbSNP

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