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rs796052938

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052938(C;C)
Make rs796052938(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29814424
GenePAGR1, PRRT2
is asnp
is mentioned by
dbSNPrs796052938
ebirs796052938
HLIrs796052938
Exacrs796052938
Varsomers796052938
Maprs796052938
PheGenIrs796052938
hapmaprs796052938
1000 genomesrs796052938
hgdprs796052938
ensemblrs796052938
gopubmedrs796052938
geneviewrs796052938
scholarrs796052938
googlers796052938
pharmgkbrs796052938
gwascentralrs796052938
openSNPrs796052938
23andMers796052938
23andMe allrs796052938
SNP Nexus

SNPshotrs796052938
SNPdbers796052938
MSV3drs796052938
GWAS Ctlgrs796052938
Max Magnitude0
ClinVar
Risk rs796052938(C;C)
Alt rs796052938(C;C)
Reference rs796052938(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAGR1 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29825745G>C
CLNSRC
CLNACC RCV000188775.2,