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

rs796052215

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052215(-;-)
Make rs796052215(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151406394
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052215
ebirs796052215
HLIrs796052215
Exacrs796052215
Varsomers796052215
Maprs796052215
PheGenIrs796052215
hapmaprs796052215
1000 genomesrs796052215
hgdprs796052215
ensemblrs796052215
gopubmedrs796052215
geneviewrs796052215
scholarrs796052215
googlers796052215
pharmgkbrs796052215
gwascentralrs796052215
openSNPrs796052215
23andMers796052215
23andMe allrs796052215
SNP Nexus

SNPshotrs796052215
SNPdbers796052215
MSV3drs796052215
GWAS Ctlgrs796052215
Max Magnitude0
ClinVar
Risk rs796052215(;)
Alt rs796052215(;)
Reference rs796052215(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151378870delT
CLNSRC
CLNACC RCV000190092.1,