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rs869312834

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312834(C;T)
Make rs869312834(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position151405188
GenePOGZ
is asnp
is mentioned by
dbSNPrs869312834
ebirs869312834
HLIrs869312834
Exacrs869312834
Varsomers869312834
Maprs869312834
PheGenIrs869312834
hapmaprs869312834
1000 genomesrs869312834
hgdprs869312834
ensemblrs869312834
gopubmedrs869312834
geneviewrs869312834
scholarrs869312834
googlers869312834
pharmgkbrs869312834
gwascentralrs869312834
openSNPrs869312834
23andMers869312834
23andMe allrs869312834
SNP Nexus

SNPshotrs869312834
SNPdbers869312834
MSV3drs869312834
GWAS Ctlgrs869312834
Max Magnitude0
ClinVar
Risk rs869312834(T;T)
Alt rs869312834(T;T)
Reference rs869312834(C;C)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151377664G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210306.1,