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rs864321668

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321668(A;A)
Make rs864321668(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406324
GenePOGZ
is asnp
is mentioned by
dbSNPrs864321668
ebirs864321668
HLIrs864321668
Exacrs864321668
Varsomers864321668
Maprs864321668
PheGenIrs864321668
hapmaprs864321668
1000 genomesrs864321668
hgdprs864321668
ensemblrs864321668
gopubmedrs864321668
geneviewrs864321668
scholarrs864321668
googlers864321668
pharmgkbrs864321668
gwascentralrs864321668
openSNPrs864321668
23andMers864321668
23andMe allrs864321668
SNP Nexus

SNPshotrs864321668
SNPdbers864321668
MSV3drs864321668
GWAS Ctlgrs864321668
Max Magnitude0
ClinVar
Risk rs864321668(A;A)
Alt rs864321668(A;A)
Reference rs864321668(T;T)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 1
HGVS NC_000001.10:g.151378800A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170496.4,