rs376319 - SNP

Select item 3763191.

rs376319 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29676856 (GRCh38)
6:29644633 (GRCh37)
Canonical SPDI:: NC_000006.12:29676855:C:T
Gene:: ZFP57 (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.213444/7611 (ALFA)
T=0.114232/61 (MGP)
T=0.134868/41 (FINRISK)
T=0.145/87 (NorthernSweden)
T=0.175926/38 (Qatari)
T=0.176339/790 (Estonian)
T=0.1875/12 (PRJEB36033)
T=0.213781/242 (Daghestan)
T=0.214709/30064 (GnomAD)
T=0.219494/2673 (GoESP)
T=0.224395/59395 (TOPMED)
T=0.232192/28020 (ExAC)
T=0.232263/57768 (GnomAD_exomes)
T=0.242718/900 (TWINSUK)
T=0.247276/953 (ALSPAC)
T=0.25/10 (GENOME_DK)
T=0.257515/257 (GoNL)
T=0.269988/1352 (1000Genomes)
T=0.277108/161 (Vietnamese)
T=0.299659/878 (KOREAN)
C=0.32963/89 (SGDP_PRJ)
T=0.375779/6298 (TOMMO)
C=0.428571/12 (Siberian)
HGVS:: NC_000006.12:g.29676856C>T, NC_000006.11:g.29644633C>T, NG_013045.1:g.5299G>A, NT_113891.3:g.1163356T>C, NT_113891.2:g.1163462T>C, NT_167249.2:g.985886C>T, NT_167249.1:g.985184C>T, NT_167247.2:g.942225C>T, NT_167247.1:g.947810C>T, NT_167248.2:g.942359C>T, NT_167248.1:g.947955C>T, NT_167245.2:g.942404C>T, NT_167245.1:g.947989C>T, NT_167246.2:g.941971C>T, NT_167246.1:g.947591C>T

Select item 1510000632.

rs151000063 has merged into rs376319 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29676856 (GRCh38)
6:29644633 (GRCh37)
Canonical SPDI:: NC_000006.12:29676855:C:T
Gene:: ZFP57 (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.213444/7611 (ALFA)
T=0.114232/61 (MGP)
T=0.134868/41 (FINRISK)
T=0.145/87 (NorthernSweden)
T=0.175926/38 (Qatari)
T=0.176339/790 (Estonian)
T=0.1875/12 (PRJEB36033)
T=0.213781/242 (Daghestan)
T=0.214709/30064 (GnomAD)
T=0.219494/2673 (GoESP)
T=0.224395/59395 (TOPMED)
T=0.232192/28020 (ExAC)
T=0.232263/57768 (GnomAD_exomes)
T=0.242718/900 (TWINSUK)
T=0.247276/953 (ALSPAC)
T=0.25/10 (GENOME_DK)
T=0.257515/257 (GoNL)
T=0.269988/1352 (1000Genomes)
T=0.277108/161 (Vietnamese)
T=0.299659/878 (KOREAN)
C=0.32963/89 (SGDP_PRJ)
T=0.375779/6298 (TOMMO)
C=0.428571/12 (Siberian)
HGVS:: NC_000006.12:g.29676856C>T, NC_000006.11:g.29644633C>T, NG_013045.1:g.5299G>A, NT_113891.3:g.1163356T>C, NT_113891.2:g.1163462T>C, NT_167249.2:g.985886C>T, NT_167249.1:g.985184C>T, NT_167247.2:g.942225C>T, NT_167247.1:g.947810C>T, NT_167248.2:g.942359C>T, NT_167248.1:g.947955C>T, NT_167245.2:g.942404C>T, NT_167245.1:g.947989C>T, NT_167246.2:g.941971C>T, NT_167246.1:g.947591C>T

Select item 1156257633.

rs115625763 has merged into rs376319 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29676856 (GRCh38)
6:29644633 (GRCh37)
Canonical SPDI:: NC_000006.12:29676855:C:T
Gene:: ZFP57 (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.213444/7611 (ALFA)
T=0.114232/61 (MGP)
T=0.134868/41 (FINRISK)
T=0.145/87 (NorthernSweden)
T=0.175926/38 (Qatari)
T=0.176339/790 (Estonian)
T=0.1875/12 (PRJEB36033)
T=0.213781/242 (Daghestan)
T=0.214709/30064 (GnomAD)
T=0.219494/2673 (GoESP)
T=0.224395/59395 (TOPMED)
T=0.232192/28020 (ExAC)
T=0.232263/57768 (GnomAD_exomes)
T=0.242718/900 (TWINSUK)
T=0.247276/953 (ALSPAC)
T=0.25/10 (GENOME_DK)
T=0.257515/257 (GoNL)
T=0.269988/1352 (1000Genomes)
T=0.277108/161 (Vietnamese)
T=0.299659/878 (KOREAN)
C=0.32963/89 (SGDP_PRJ)
T=0.375779/6298 (TOMMO)
C=0.428571/12 (Siberian)
HGVS:: NC_000006.12:g.29676856C>T, NC_000006.11:g.29644633C>T, NG_013045.1:g.5299G>A, NT_113891.3:g.1163356T>C, NT_113891.2:g.1163462T>C, NT_167249.2:g.985886C>T, NT_167249.1:g.985184C>T, NT_167247.2:g.942225C>T, NT_167247.1:g.947810C>T, NT_167248.2:g.942359C>T, NT_167248.1:g.947955C>T, NT_167245.2:g.942404C>T, NT_167245.1:g.947989C>T, NT_167246.2:g.941971C>T, NT_167246.1:g.947591C>T

dbSNP