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rs796052218

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052218(C;T)
Make rs796052218(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406004
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052218
ebirs796052218
HLIrs796052218
Exacrs796052218
Varsomers796052218
Maprs796052218
PheGenIrs796052218
hapmaprs796052218
1000 genomesrs796052218
hgdprs796052218
ensemblrs796052218
gopubmedrs796052218
geneviewrs796052218
scholarrs796052218
googlers796052218
pharmgkbrs796052218
gwascentralrs796052218
openSNPrs796052218
23andMers796052218
23andMe allrs796052218
SNP Nexus

SNPshotrs796052218
SNPdbers796052218
MSV3drs796052218
GWAS Ctlgrs796052218
Max Magnitude0
ClinVar
Risk rs796052218(T;T)
Alt rs796052218(T;T)
Reference rs796052218(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151378480G>A
CLNSRC
CLNACC RCV000190091.1,