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rs796052219

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052219(-;-)
Make rs796052219(-;AACT)
Make rs796052219(AACT;AACT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151408545
GenePOGZ
is asnp
is mentioned by
dbSNPrs796052219
ebirs796052219
HLIrs796052219
Exacrs796052219
Varsomers796052219
Maprs796052219
PheGenIrs796052219
hapmaprs796052219
1000 genomesrs796052219
hgdprs796052219
ensemblrs796052219
gopubmedrs796052219
geneviewrs796052219
scholarrs796052219
googlers796052219
pharmgkbrs796052219
gwascentralrs796052219
openSNPrs796052219
23andMers796052219
23andMe allrs796052219
SNP Nexus

SNPshotrs796052219
SNPdbers796052219
MSV3drs796052219
GWAS Ctlgrs796052219
Max Magnitude0
ClinVar
Risk rs796052219(AACT;AACT)
Alt rs796052219(AACT;AACT)
Reference rs796052219(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151381022_151381025dupAGTT
CLNSRC
CLNACC RCV000190095.1,