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rs796052221

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052221(-;-)
Make rs796052221(-;C)
Make rs796052221(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406941
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052221
ebirs796052221
HLIrs796052221
Exacrs796052221
Varsomers796052221
Maprs796052221
PheGenIrs796052221
hapmaprs796052221
1000 genomesrs796052221
hgdprs796052221
ensemblrs796052221
gopubmedrs796052221
geneviewrs796052221
scholarrs796052221
googlers796052221
pharmgkbrs796052221
gwascentralrs796052221
openSNPrs796052221
23andMers796052221
23andMe allrs796052221
SNP Nexus

SNPshotrs796052221
SNPdbers796052221
MSV3drs796052221
GWAS Ctlgrs796052221
Max Magnitude0
ClinVar
Risk rs796052221(C;C)
Alt rs796052221(C;C)
Reference rs796052221(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151379418dupG
CLNSRC
CLNACC RCV000190097.1,