SNP Links for Gene (Select 406890) - SNP

Links from Gene

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Select item 14894474931.

rs1489447493 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:52269495 (GRCh38)
3:52303511 (GRCh37)
Canonical SPDI:: NC_000003.12:52269494:C:A,NC_000003.12:52269494:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.52269495C>A, NC_000003.12:g.52269495C>T, NC_000003.11:g.52303511C>A, NC_000003.11:g.52303511C>T

Select item 14879060302.

rs1487906030 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 3:52270047 (GRCh38)
3:52304064 (GRCh37)
Canonical SPDI:: NC_000003.12:52270047:T:TT
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.52270048dup, NC_000003.11:g.52304064dup

Select item 14873533233.

rs1487353323 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:52269931 (GRCh38)
3:52303947 (GRCh37)
Canonical SPDI:: NC_000003.12:52269930:T:C
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,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_000003.12:g.52269931T>C, NC_000003.11:g.52303947T>C

Select item 14859450484.

rs1485945048 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52269199 (GRCh38)
3:52303215 (GRCh37)
Canonical SPDI:: NC_000003.12:52269198:G:A
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000003.12:g.52269199G>A, NC_000003.11:g.52303215G>A

Select item 14831799965.

rs1483179996 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52268756 (GRCh38)
3:52302772 (GRCh37)
Canonical SPDI:: NC_000003.12:52268755:G:A
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000022/3 (GnomAD)
HGVS:: NC_000003.12:g.52268756G>A, NC_000003.11:g.52302772G>A

Select item 14830068796.

rs1483006879 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAGG [Show Flanks]
Chromosome:: 3:52269703 (GRCh38)
3:52303720 (GRCh37)
Canonical SPDI:: NC_000003.12:52269703:TAGG:TAGGTAGG
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAGGTAGG=0./0 (ALFA)
TAGG=0.000004/1 (TOPMED)
TAGG=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.52269704_52269707dup, NC_000003.11:g.52303720_52303723dup

Select item 14810388217.

rs1481038821 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52268854 (GRCh38)
3:52302870 (GRCh37)
Canonical SPDI:: NC_000003.12:52268853:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.52268854C>T, NC_000003.11:g.52302870C>T

Select item 14804942918.

rs1480494291 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:52268091 (GRCh38)
3:52302107 (GRCh37)
Canonical SPDI:: NC_000003.12:52268090:A:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.52268091A>T, NC_000003.11:g.52302107A>T

Select item 14793737389.

rs1479373738 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52270029 (GRCh38)
3:52304045 (GRCh37)
Canonical SPDI:: NC_000003.12:52270028:G:A
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000003.12:g.52270029G>A, NC_000003.11:g.52304045G>A

Select item 147711352410.

rs1477113524 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52268050 (GRCh38)
3:52302066 (GRCh37)
Canonical SPDI:: NC_000003.12:52268049:G:A
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000026/7 (TOPMED)
HGVS:: NC_000003.12:g.52268050G>A, NC_000003.11:g.52302066G>A

Select item 147702143111.

rs1477021431 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52269698 (GRCh38)
3:52303714 (GRCh37)
Canonical SPDI:: NC_000003.12:52269697:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_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_000003.12:g.52269698C>T, NC_000003.11:g.52303714C>T

Select item 147587176512.

rs1475871765 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:52268783 (GRCh38)
3:52302799 (GRCh37)
Canonical SPDI:: NC_000003.12:52268782:C:A
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000003.12:g.52268783C>A, NC_000003.11:g.52302799C>A

Select item 147522599813.

rs1475225998 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52268169 (GRCh38)
3:52302185 (GRCh37)
Canonical SPDI:: NC_000003.12:52268168:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,intron_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_000003.12:g.52268169C>T, NC_000003.11:g.52302185C>T

Select item 147483971914.

rs1474839719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52269661 (GRCh38)
3:52303677 (GRCh37)
Canonical SPDI:: NC_000003.12:52269660:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000003.12:g.52269661C>T, NC_000003.11:g.52303677C>T

Select item 147380174315.

rs1473801743 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:52268546 (GRCh38)
3:52302562 (GRCh37)
Canonical SPDI:: NC_000003.12:52268545:A:G
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.52268546A>G, NC_000003.11:g.52302562A>G

Select item 147307176316.

rs1473071763 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:52270267 (GRCh38)
3:52304283 (GRCh37)
Canonical SPDI:: NC_000003.12:52270266:G:A,NC_000003.12:52270266:G:C
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.52270267G>A, NC_000003.12:g.52270267G>C, NC_000003.11:g.52304283G>A, NC_000003.11:g.52304283G>C

Select item 147074641817.

rs1470746418 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:52267927 (GRCh38)
3:52301943 (GRCh37)
Canonical SPDI:: NC_000003.12:52267926:G:C
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,500B_downstream_variant,downstream_transcript_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_000003.12:g.52267927G>C, NC_000003.11:g.52301943G>C

Select item 146992672918.

rs1469926729 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:52267838 (GRCh38)
3:52301854 (GRCh37)
Canonical SPDI:: NC_000003.12:52267837:A:G
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,500B_downstream_variant,downstream_transcript_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_000003.12:g.52267838A>G, NC_000003.11:g.52301854A>G

Select item 146984699819.

rs1469846998 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52268971 (GRCh38)
3:52302987 (GRCh37)
Canonical SPDI:: NC_000003.12:52268970:C:T
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.52268971C>T, NC_000003.11:g.52302987C>T

Select item 146927890620.

rs1469278906 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:52268607 (GRCh38)
3:52302623 (GRCh37)
Canonical SPDI:: NC_000003.12:52268606:T:C
Gene:: WDR82 (Varview), MIRLET7G (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.52268607T>C, NC_000003.11:g.52302623T>C

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