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rs796052220

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796052220(-;-)
Make rs796052220(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151408447
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052220
ebirs796052220
HLIrs796052220
Exacrs796052220
Varsomers796052220
Maprs796052220
PheGenIrs796052220
hapmaprs796052220
1000 genomesrs796052220
hgdprs796052220
ensemblrs796052220
gopubmedrs796052220
geneviewrs796052220
scholarrs796052220
googlers796052220
pharmgkbrs796052220
gwascentralrs796052220
openSNPrs796052220
23andMers796052220
23andMe allrs796052220
SNP Nexus

SNPshotrs796052220
SNPdbers796052220
MSV3drs796052220
GWAS Ctlgrs796052220
Max Magnitude0
ClinVar
Risk rs796052220(;)
Alt rs796052220(;)
Reference rs796052220(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151380923_151380924delAG
CLNSRC
CLNACC RCV000190096.2,