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rs1057519392

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519392(C;C)
Make rs1057519392(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position151412348
GenePOGZ
is asnp
is mentioned by
dbSNPrs1057519392
dbSNP (old)rs1057519392
ClinGenrs1057519392
ebirs1057519392
HLIrs1057519392
Exacrs1057519392
Gnomadrs1057519392
Varsomers1057519392
Maprs1057519392
PheGenIrs1057519392
Biobankrs1057519392
1000 genomesrs1057519392
hgdprs1057519392
ensemblrs1057519392
gopubmedrs1057519392
geneviewrs1057519392
scholarrs1057519392
googlers1057519392
pharmgkbrs1057519392
gwascentralrs1057519392
openSNPrs1057519392
23andMers1057519392
23andMe allrs1057519392
SNPshotrs1057519392
SNPdbers1057519392
MSV3drs1057519392
GWAS Ctlgrs1057519392
Max Magnitude0
ClinVar
Risk rs1057519392(C;C)
Alt rs1057519392(C;C)
Reference Rs1057519392(T;T)
Significance Probable-Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151384824A>G
CLNSRC
CLNACC RCV000417037.1,