SNP Links for Gene (Select 9640) - SNP

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Select item 14915707781.

rs1491570778 has merged into rs10667788 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 15:84766721 (GRCh38)
15:85309952 (GRCh37)
Canonical SPDI:: NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000015.10:84766706:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTGTGTGT=0./0 (ALFA)
GTGTGTGTGTGT=0.225/9 (GENOME_DK)
HGVS:: NC_000015.10:g.84766707GT[7], NC_000015.10:g.84766707GT[8], NC_000015.10:g.84766707GT[9], NC_000015.10:g.84766707GT[10], NC_000015.10:g.84766707GT[11], NC_000015.10:g.84766707GT[12], NC_000015.10:g.84766707GT[13], NC_000015.10:g.84766707GT[14], NC_000015.10:g.84766707GT[15], NC_000015.10:g.84766707GT[16], NC_000015.10:g.84766707GT[18], NC_000015.10:g.84766707GT[19], NC_000015.10:g.84766707GT[20], NC_000015.10:g.84766707GT[21], NC_000015.10:g.84766707GT[22], NC_000015.10:g.84766707GT[23], NC_000015.10:g.84766707GT[24], NC_000015.10:g.84766707GT[25], NC_000015.10:g.84766707GT[26], NC_000015.10:g.84766707GT[27], NC_000015.10:g.84766707GT[28], NC_000015.9:g.85309938GT[7], NC_000015.9:g.85309938GT[8], NC_000015.9:g.85309938GT[9], NC_000015.9:g.85309938GT[10], NC_000015.9:g.85309938GT[11], NC_000015.9:g.85309938GT[12], NC_000015.9:g.85309938GT[13], NC_000015.9:g.85309938GT[14], NC_000015.9:g.85309938GT[15], NC_000015.9:g.85309938GT[16], NC_000015.9:g.85309938GT[18], NC_000015.9:g.85309938GT[19], NC_000015.9:g.85309938GT[20], NC_000015.9:g.85309938GT[21], NC_000015.9:g.85309938GT[22], NC_000015.9:g.85309938GT[23], NC_000015.9:g.85309938GT[24], NC_000015.9:g.85309938GT[25], NC_000015.9:g.85309938GT[26], NC_000015.9:g.85309938GT[27], NC_000015.9:g.85309938GT[28], NG_028094.2:g.23121GT[7], NG_028094.2:g.23121GT[8], NG_028094.2:g.23121GT[9], NG_028094.2:g.23121GT[10], NG_028094.2:g.23121GT[11], NG_028094.2:g.23121GT[12], NG_028094.2:g.23121GT[13], NG_028094.2:g.23121GT[14], NG_028094.2:g.23121GT[15], NG_028094.2:g.23121GT[16], NG_028094.2:g.23121GT[18], NG_028094.2:g.23121GT[19], NG_028094.2:g.23121GT[20], NG_028094.2:g.23121GT[21], NG_028094.2:g.23121GT[22], NG_028094.2:g.23121GT[23], NG_028094.2:g.23121GT[24], NG_028094.2:g.23121GT[25], NG_028094.2:g.23121GT[26], NG_028094.2:g.23121GT[27], NG_028094.2:g.23121GT[28]

Select item 14915429212.

rs1491542921 has merged into rs61292759 [Homo sapiens]

Variant type:: DELINS
Alleles:: AC>- [Show Flanks]
Chromosome:: 15:84759967 (GRCh38)
15:85303198 (GRCh37)
Canonical SPDI:: NC_000015.10:84759965:CAC:C
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.03507/416 (ALFA)
-=0.01099/6 (NorthernSweden)
-=0.08533/1205 (TOMMO)
-=0.09502/2808 (GnomAD)
HGVS:: NC_000015.10:g.84759967_84759968del, NC_000015.9:g.85303198_85303199del, NG_028094.2:g.16381_16382del

Select item 14915296603.

rs1491529660 [Homo sapiens]

Variant type:: INS
Alleles:: ->CG,CT,T [Show Flanks]
Chromosome:: 15:84759966 (GRCh38)
15:85303198 (GRCh37)
Canonical SPDI:: NC_000015.10:84759966::CG,NC_000015.10:84759966::CT,NC_000015.10:84759966::T
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CT=0./0 (ALFA)
CT=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.84759966_84759967insCG, NC_000015.10:g.84759966_84759967insCT, NC_000015.10:g.84759966_84759967insT, NC_000015.9:g.85303197_85303198insCG, NC_000015.9:g.85303197_85303198insCT, NC_000015.9:g.85303197_85303198insT, NG_028094.2:g.16380_16381insCG, NG_028094.2:g.16380_16381insCT, NG_028094.2:g.16380_16381insT

Select item 14915022674.

rs1491502267 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATGTGTGT [Show Flanks]
Chromosome:: 15:84766707 (GRCh38)
15:85309939 (GRCh37)
Canonical SPDI:: NC_000015.10:84766707:TGTGTGT:TGTGTGTATGTGTGT
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGTGTGTATGTGTGT=0.00008/1 (ALFA)
TGTGTGTA=0.0013/2 (GnomAD)
HGVS:: NC_000015.10:g.84766708_84766714TG[3]TATGTGTGT[1], NC_000015.9:g.85309939_85309945TG[3]TATGTGTGT[1], NG_028094.2:g.23122_23128TG[3]TATGTGTGT[1]

Select item 14914956775.

rs1491495677 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACCCCC [Show Flanks]
Chromosome:: 15:84790098 (GRCh38)
15:85333330 (GRCh37)
Canonical SPDI:: NC_000015.10:84790098:ACCCCCACCCCC:ACCCCCACCCCCACCCCC
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACCCCCACCCCCACCCCC=0./0 (ALFA)
ACCCCC=0.00029/2 (GnomAD)
HGVS:: NC_000015.10:g.84790099ACCCCC[3], NC_000015.9:g.85333330ACCCCC[3], NG_028094.2:g.46513ACCCCC[3]

Select item 14914808736.

rs1491480873 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 15:84764910 (GRCh38)
15:85308141 (GRCh37)
Canonical SPDI:: NC_000015.10:84764908:TGT:T
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000253/3 (ALFA)
-=0.000416/110 (TOPMED)
-=0.000822/62 (GnomAD)
-=0.000937/6 (1000Genomes)
HGVS:: NC_000015.10:g.84764910_84764911del, NC_000015.9:g.85308141_85308142del, NG_028094.2:g.21324_21325del

Select item 14914316237.

rs1491431623 has merged into rs11313287 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTTTTT,TTTTTTTTTTT [Show Flanks]
Chromosome:: 15:84764918 (GRCh38)
15:85308149 (GRCh37)
Canonical SPDI:: NC_000015.10:84764910:TTTTTTTTT:TTTTTTT,NC_000015.10:84764910:TTTTTTTTT:TTTTTTTT,NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTT,NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTT,NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:84764910:TTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
T=0.142971/716 (1000Genomes)
T=0.435449/115259 (TOPMED)
-=0.477891/281 (NorthernSweden)
HGVS:: NC_000015.10:g.84764918_84764919del, NC_000015.10:g.84764919del, NC_000015.10:g.84764919dup, NC_000015.10:g.84764918_84764919dup, NC_000015.10:g.84764914_84764919dup, NC_000015.10:g.84764911_84764919dup, NC_000015.9:g.85308149_85308150del, NC_000015.9:g.85308150del, NC_000015.9:g.85308150dup, NC_000015.9:g.85308149_85308150dup, NC_000015.9:g.85308145_85308150dup, NC_000015.9:g.85308142_85308150dup, NG_028094.2:g.21332_21333del, NG_028094.2:g.21333del, NG_028094.2:g.21333dup, NG_028094.2:g.21332_21333dup, NG_028094.2:g.21328_21333dup, NG_028094.2:g.21325_21333dup

Select item 14914171998.

rs1491417199 has merged into rs36104262 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 15:84754977 (GRCh38)
15:85298208 (GRCh37)
Canonical SPDI:: NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:84754963:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.25/10 (GENOME_DK)
HGVS:: NC_000015.10:g.84754977_84754982del, NC_000015.10:g.84754979_84754982del, NC_000015.10:g.84754980_84754982del, NC_000015.10:g.84754981_84754982del, NC_000015.10:g.84754982del, NC_000015.10:g.84754982dup, NC_000015.10:g.84754981_84754982dup, NC_000015.10:g.84754980_84754982dup, NC_000015.10:g.84754979_84754982dup, NC_000015.10:g.84754978_84754982dup, NC_000015.10:g.84754977_84754982dup, NC_000015.10:g.84754976_84754982dup, NC_000015.9:g.85298208_85298213del, NC_000015.9:g.85298210_85298213del, NC_000015.9:g.85298211_85298213del, NC_000015.9:g.85298212_85298213del, NC_000015.9:g.85298213del, NC_000015.9:g.85298213dup, NC_000015.9:g.85298212_85298213dup, NC_000015.9:g.85298211_85298213dup, NC_000015.9:g.85298210_85298213dup, NC_000015.9:g.85298209_85298213dup, NC_000015.9:g.85298208_85298213dup, NC_000015.9:g.85298207_85298213dup, NG_028094.2:g.11391_11396del, NG_028094.2:g.11393_11396del, NG_028094.2:g.11394_11396del, NG_028094.2:g.11395_11396del, NG_028094.2:g.11396del, NG_028094.2:g.11396dup, NG_028094.2:g.11395_11396dup, NG_028094.2:g.11394_11396dup, NG_028094.2:g.11393_11396dup, NG_028094.2:g.11392_11396dup, NG_028094.2:g.11391_11396dup, NG_028094.2:g.11390_11396dup

Select item 14913862909.

rs1491386290 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 15:84796221 (GRCh38)
15:85339452 (GRCh37)
Canonical SPDI:: NC_000015.10:84796220:CA:
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000015.10:g.84796221_84796222del, NC_000015.9:g.85339452_85339453del, NG_028094.2:g.52635_52636del

Select item 149122899210.

rs1491228992 has merged into rs1165913540 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA [Show Flanks]
Chromosome:: 15:84796286 (GRCh38)
15:85339517 (GRCh37)
Canonical SPDI:: NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000015.10:84796267:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATATATA=0./0 (ALFA)
-=0.01333/215 (TOMMO)
HGVS:: NC_000015.10:g.84796268TA[9], NC_000015.10:g.84796268TA[10], NC_000015.10:g.84796268TA[11], NC_000015.10:g.84796268TA[12], NC_000015.10:g.84796268TA[13], NC_000015.10:g.84796268TA[15], NC_000015.10:g.84796268TA[16], NC_000015.10:g.84796268TA[17], NC_000015.10:g.84796268TA[18], NC_000015.10:g.84796268TA[19], NC_000015.10:g.84796268TA[20], NC_000015.10:g.84796268TA[21], NC_000015.10:g.84796268TA[22], NC_000015.10:g.84796268TA[23], NC_000015.10:g.84796268TA[24], NC_000015.10:g.84796268TA[25], NC_000015.10:g.84796268TA[26], NC_000015.9:g.85339499TA[9], NC_000015.9:g.85339499TA[10], NC_000015.9:g.85339499TA[11], NC_000015.9:g.85339499TA[12], NC_000015.9:g.85339499TA[13], NC_000015.9:g.85339499TA[15], NC_000015.9:g.85339499TA[16], NC_000015.9:g.85339499TA[17], NC_000015.9:g.85339499TA[18], NC_000015.9:g.85339499TA[19], NC_000015.9:g.85339499TA[20], NC_000015.9:g.85339499TA[21], NC_000015.9:g.85339499TA[22], NC_000015.9:g.85339499TA[23], NC_000015.9:g.85339499TA[24], NC_000015.9:g.85339499TA[25], NC_000015.9:g.85339499TA[26], NG_028094.2:g.52682TA[9], NG_028094.2:g.52682TA[10], NG_028094.2:g.52682TA[11], NG_028094.2:g.52682TA[12], NG_028094.2:g.52682TA[13], NG_028094.2:g.52682TA[15], NG_028094.2:g.52682TA[16], NG_028094.2:g.52682TA[17], NG_028094.2:g.52682TA[18], NG_028094.2:g.52682TA[19], NG_028094.2:g.52682TA[20], NG_028094.2:g.52682TA[21], NG_028094.2:g.52682TA[22], NG_028094.2:g.52682TA[23], NG_028094.2:g.52682TA[24], NG_028094.2:g.52682TA[25], NG_028094.2:g.52682TA[26]

Select item 149122176811.

rs1491221768 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 15:84750538 (GRCh38)
15:85293770 (GRCh37)
Canonical SPDI:: NC_000015.10:84750538:GGGG:GGGGG
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGG=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.84750542dup, NC_000015.9:g.85293773dup, NG_028094.2:g.6956dup

Select item 149115594212.

rs1491155942 [Homo sapiens]

Variant type:: INS
Alleles:: ->TC [Show Flanks]
Chromosome:: 15:84796268 (GRCh38)
15:85339500 (GRCh37)
Canonical SPDI:: NC_000015.10:84796268::TC
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TC=0./0 (ALFA)
HGVS:: NC_000015.10:g.84796268_84796269insTC, NC_000015.9:g.85339499_85339500insTC, NG_028094.2:g.52682_52683insTC

Select item 149115505313.

rs1491155053 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 15:84750538 (GRCh38)
15:85293769 (GRCh37)
Canonical SPDI:: NC_000015.10:84750537:AG:
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.84750538_84750539del, NC_000015.9:g.85293769_85293770del, NG_028094.2:g.6952_6953del

Select item 149114104714.

rs1491141047 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 15:84795522 (GRCh38)
15:85338753 (GRCh37)
Canonical SPDI:: NC_000015.10:84795521:AT:
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84795522_84795523del, NC_000015.9:g.85338753_85338754del, NG_028094.2:g.51936_51937del

Select item 149110565015.

rs1491105650 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 15:84795522 (GRCh38)
15:85338754 (GRCh37)
Canonical SPDI:: NC_000015.10:84795522:T:TT
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.84795523dup, NC_000015.9:g.85338754dup, NG_028094.2:g.51937dup

Select item 149110256116.

rs1491102561 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 15:84790098 (GRCh38)
15:85333329 (GRCh37)
Canonical SPDI:: NC_000015.10:84790097:AA:
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.001097/18 (TOMMO)
-=0.001099/149 (GnomAD)
HGVS:: NC_000015.10:g.84790098_84790099del, NC_000015.9:g.85333329_85333330del, NG_028094.2:g.46512_46513del

Select item 149105795917.

rs1491057959 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 15:84775410 (GRCh38)
15:85318641 (GRCh37)
Canonical SPDI:: NC_000015.10:84775409:TT:
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: -=0.00005/4 (GnomAD)
HGVS:: NC_000015.10:g.84775410_84775411del, NC_000015.9:g.85318641_85318642del, NG_028094.2:g.31824_31825del

Select item 149104652618.

rs1491046526 has merged into rs35020131 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 15:84785877 (GRCh38)
15:85329108 (GRCh37)
Canonical SPDI:: NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:84785865:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
A=0.21115/125 (NorthernSweden)
HGVS:: NC_000015.10:g.84785877_84785880del, NC_000015.10:g.84785878_84785880del, NC_000015.10:g.84785879_84785880del, NC_000015.10:g.84785880del, NC_000015.10:g.84785880dup, NC_000015.10:g.84785879_84785880dup, NC_000015.10:g.84785880_84785881insAAAAAAAAAAAAAAAA, NC_000015.9:g.85329108_85329111del, NC_000015.9:g.85329109_85329111del, NC_000015.9:g.85329110_85329111del, NC_000015.9:g.85329111del, NC_000015.9:g.85329111dup, NC_000015.9:g.85329110_85329111dup, NC_000015.9:g.85329111_85329112insAAAAAAAAAAAAAAAA, NG_028094.2:g.42291_42294del, NG_028094.2:g.42292_42294del, NG_028094.2:g.42293_42294del, NG_028094.2:g.42294del, NG_028094.2:g.42294dup, NG_028094.2:g.42293_42294dup, NG_028094.2:g.42294_42295insAAAAAAAAAAAAAAAA

Select item 149095185919.

rs1490951859 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:84762989 (GRCh38)
15:85306220 (GRCh37)
Canonical SPDI:: NC_000015.10:84762988:A:G
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000057/8 (GnomAD)
G=0.000068/18 (TOPMED)
HGVS:: NC_000015.10:g.84762989A>G, NC_000015.9:g.85306220A>G, NG_028094.2:g.19403A>G

Select item 149093495320.

rs1490934953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:84751650 (GRCh38)
15:85294881 (GRCh37)
Canonical SPDI:: NC_000015.10:84751649:A:G
Gene:: ZNF592 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84751650A>G, NC_000015.9:g.85294881A>G, NG_028094.2:g.8064A>G

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