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rs864321674

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321674(C;T)
Make rs864321674(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406100
GenePOGZ
is asnp
is mentioned by
dbSNPrs864321674
ebirs864321674
HLIrs864321674
Exacrs864321674
Varsomers864321674
Maprs864321674
PheGenIrs864321674
hapmaprs864321674
1000 genomesrs864321674
hgdprs864321674
ensemblrs864321674
gopubmedrs864321674
geneviewrs864321674
scholarrs864321674
googlers864321674
pharmgkbrs864321674
gwascentralrs864321674
openSNPrs864321674
23andMers864321674
23andMe allrs864321674
SNP Nexus

SNPshotrs864321674
SNPdbers864321674
MSV3drs864321674
GWAS Ctlgrs864321674
Max Magnitude0
ClinVar
Risk rs864321674(T;T)
Alt rs864321674(T;T)
Reference rs864321674(C;C)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151378576G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203580.1,