SNP Links for Gene (Select 102724875) - SNP

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Items: 1 to 20 of 36

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Select item 14753655421.

rs1475365542 [Homo sapiens]

Variant type:: SNV:
Alleles:: CT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 14193487642.

rs1419348764 [Homo sapiens]

Variant type:: SNV:
Alleles:: CTTTCTT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 13662860103.

rs1366286010 [Homo sapiens]

Variant type:: SNV:
Alleles:: CTT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 11637586714.

rs1163758671 [Homo sapiens]

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

Select item 10240216435.

rs1024021643 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:110507170 (GRCh38)
2:111264747 (GRCh37)
Canonical SPDI:: NC_000002.12:110507169:A:C
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.5/1 (Siberian)
HGVS:: NC_000002.12:g.110507170A>C, NC_000002.11:g.111264747A>C

Select item 10140104276.

rs1014010427 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:110493106 (GRCh38)
2:111250683 (GRCh37)
Canonical SPDI:: NC_000002.12:110493105:A:G
Gene:: LOC102724875 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: A=0.5/1 (Siberian)
HGVS:: NC_000002.12:g.110493106A>G, NC_000002.11:g.111250683A>G

Select item 9584772817.

rs958477281 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:110493091 (GRCh38)
2:111250668 (GRCh37)
Canonical SPDI:: NC_000002.12:110493090:G:A
Gene:: LOC102724875 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.5/1 (Siberian)
HGVS:: NC_000002.12:g.110493091G>A, NC_000002.11:g.111250668G>A

Select item 8799421418.

rs879942141 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:110507203 (GRCh38)
2:111264780 (GRCh37)
Canonical SPDI:: NC_000002.12:110507202:C:T
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000002.12:g.110507203C>T, NC_000002.11:g.111264780C>T

Select item 7639655629.

rs763965562 has merged into rs57178264 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTTCTTTCTTT>-,CTTTCTTT [Show Flanks]
Chromosome:: 2:110501560 (GRCh38)
2:111259137 (GRCh37)
Canonical SPDI:: NC_000002.12:110501512:TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT:TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000002.12:110501512:TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT:TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: TTTC=0.0345/128 (TWINSUK)
TTTC=0.0348/134 (ALSPAC)
HGVS:: NC_000002.12:g.110501516CTTT[11], NC_000002.12:g.110501516CTTT[13], NC_000002.11:g.111259093CTTT[11], NC_000002.11:g.111259093CTTT[13]

Select item 20211929310.

rs202119293 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 2:110511536 (GRCh38)
2:111269114 (GRCh37)
Canonical SPDI:: NC_000002.12:110511536:TTTT:TTTTT
Gene:: LOC102724875 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000002.12:g.110511540dup, NC_000002.11:g.111269117dup, XR_427156.5:n.543dup, XR_427156.2:n.510dup

Select item 20211850911.

rs202118509 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:110510937 (GRCh38)
2:111268514 (GRCh37)
Canonical SPDI:: NC_000002.12:110510936:T:G
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110510937T>G, NC_000002.11:g.111268514T>G

Select item 20151573112.

rs201515731 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:110511185 (GRCh38)
2:111268762 (GRCh37)
Canonical SPDI:: NC_000002.12:110511184:G:T
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000002.12:g.110511185G>T, NC_000002.11:g.111268762G>T

Select item 20044582213.

rs200445822 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:110510939 (GRCh38)
2:111268516 (GRCh37)
Canonical SPDI:: NC_000002.12:110510938:T:G
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110510939T>G, NC_000002.11:g.111268516T>G

Select item 11375797414.

rs113757974 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:110501800 (GRCh38)
2:111259377 (GRCh37)
Canonical SPDI:: NC_000002.12:110501799:C:T
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110501800C>T, NC_000002.11:g.111259377C>T

Select item 11374033015.

rs113740330 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:110499432 (GRCh38)
2:111257009 (GRCh37)
Canonical SPDI:: NC_000002.12:110499431:C:T
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110499432C>T, NC_000002.11:g.111257009C>T

Select item 11310702816.

rs113107028 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:110504725 (GRCh38)
2:111262302 (GRCh37)
Canonical SPDI:: NC_000002.12:110504724:T:C
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110504725T>C, NC_000002.11:g.111262302T>C

Select item 11211552717.

rs112115527 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:110501891 (GRCh38)
2:111259468 (GRCh37)
Canonical SPDI:: NC_000002.12:110501890:A:G
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110501891A>G, NC_000002.11:g.111259468A>G

Select item 11200516718.

rs112005167 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:110508506 (GRCh38)
2:111266083 (GRCh37)
Canonical SPDI:: NC_000002.12:110508505:A:C
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110508506A>C, NC_000002.11:g.111266083A>C

Select item 6145828419.

rs61458284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:110501201 (GRCh38)
2:111258778 (GRCh37)
Canonical SPDI:: NC_000002.12:110501200:G:C
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110501201G>C, NC_000002.11:g.111258778G>C

Select item 6134385120.

rs61343851 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:110501121 (GRCh38)
2:111258698 (GRCh37)
Canonical SPDI:: NC_000002.12:110501120:A:C
Gene:: LOC102724875 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.110501121A>C, NC_000002.11:g.111258698A>C

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