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rs796052937

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052937(A;T)
Make rs796052937(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29814393
GenePAGR1, PRRT2
is asnp
is mentioned by
dbSNPrs796052937
ebirs796052937
HLIrs796052937
Exacrs796052937
Varsomers796052937
Maprs796052937
PheGenIrs796052937
hapmaprs796052937
1000 genomesrs796052937
hgdprs796052937
ensemblrs796052937
gopubmedrs796052937
geneviewrs796052937
scholarrs796052937
googlers796052937
pharmgkbrs796052937
gwascentralrs796052937
openSNPrs796052937
23andMers796052937
23andMe allrs796052937
SNP Nexus

SNPshotrs796052937
SNPdbers796052937
MSV3drs796052937
GWAS Ctlgrs796052937
Max Magnitude0
ClinVar
Risk rs796052937(T;T)
Alt rs796052937(T;T)
Reference rs796052937(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PAGR1 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29825714A>T
CLNSRC
CLNACC RCV000188774.1,