Have questions? Visit https://www.reddit.com/r/SNPedia

rs756659230

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756659230(G;T)
Make rs756659230(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position151406445
GenePOGZ
is asnp
is mentioned by
dbSNPrs756659230
ebirs756659230
HLIrs756659230
Exacrs756659230
Varsomers756659230
Maprs756659230
PheGenIrs756659230
hapmaprs756659230
1000 genomesrs756659230
hgdprs756659230
ensemblrs756659230
gopubmedrs756659230
geneviewrs756659230
scholarrs756659230
googlers756659230
pharmgkbrs756659230
gwascentralrs756659230
openSNPrs756659230
23andMers756659230
23andMe allrs756659230
SNP Nexus

SNPshotrs756659230
SNPdbers756659230
MSV3drs756659230
GWAS Ctlgrs756659230
Max Magnitude0
ClinVar
Risk rs756659230(T;T)
Alt rs756659230(T;T)
Reference rs756659230(G;G)
Significance Pathogenic
Disease White-sutton syndrome
Variation info
Gene POGZ
CLNDBN White-sutton syndrome
Reversed 0
HGVS NC_000001.10:g.151378921G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210329.1,