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rs796052936

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052936(A;A)
Make rs796052936(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29813926
GenePRRT2
is asnp
is mentioned by
dbSNPrs796052936
ebirs796052936
HLIrs796052936
Exacrs796052936
Varsomers796052936
Maprs796052936
PheGenIrs796052936
hapmaprs796052936
1000 genomesrs796052936
hgdprs796052936
ensemblrs796052936
gopubmedrs796052936
geneviewrs796052936
scholarrs796052936
googlers796052936
pharmgkbrs796052936
gwascentralrs796052936
openSNPrs796052936
23andMers796052936
23andMe allrs796052936
SNP Nexus

SNPshotrs796052936
SNPdbers796052936
MSV3drs796052936
GWAS Ctlgrs796052936
Max Magnitude0
ClinVar
Risk rs796052936(A;A)
Alt rs796052936(A;A)
Reference rs796052936(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC100289283 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29825247C>A
CLNSRC
CLNACC RCV000188772.2,