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

rs796052217

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052217(-;-)
Make rs796052217(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151405994
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052217
ebirs796052217
HLIrs796052217
Exacrs796052217
Varsomers796052217
Maprs796052217
PheGenIrs796052217
hapmaprs796052217
1000 genomesrs796052217
hgdprs796052217
ensemblrs796052217
gopubmedrs796052217
geneviewrs796052217
scholarrs796052217
googlers796052217
pharmgkbrs796052217
gwascentralrs796052217
openSNPrs796052217
23andMers796052217
23andMe allrs796052217
SNP Nexus

SNPshotrs796052217
SNPdbers796052217
MSV3drs796052217
GWAS Ctlgrs796052217
Max Magnitude0
ClinVar
Risk rs796052217(;)
Alt rs796052217(;)
Reference rs796052217(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151378470delT
CLNSRC
CLNACC RCV000190094.1,