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rs796052216

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052216(-;-)
Make rs796052216(-;C)
Make rs796052216(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406284
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052216
ebirs796052216
HLIrs796052216
Exacrs796052216
Varsomers796052216
Maprs796052216
PheGenIrs796052216
hapmaprs796052216
1000 genomesrs796052216
hgdprs796052216
ensemblrs796052216
gopubmedrs796052216
geneviewrs796052216
scholarrs796052216
googlers796052216
pharmgkbrs796052216
gwascentralrs796052216
openSNPrs796052216
23andMers796052216
23andMe allrs796052216
SNP Nexus

SNPshotrs796052216
SNPdbers796052216
MSV3drs796052216
GWAS Ctlgrs796052216
Max Magnitude0
ClinVar
Risk rs796052216(C;C)
Alt rs796052216(C;C)
Reference rs796052216(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151378761dupG
CLNSRC
CLNACC RCV000190093.1,