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rs796052943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs796052943(-;-)
Make rs796052943(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29813269
GenePRRT2
is asnp
is mentioned by
dbSNPrs796052943
dbSNP (classic)rs796052943
ClinGenrs796052943
ebirs796052943
HLIrs796052943
Exacrs796052943
Gnomadrs796052943
Varsomers796052943
LitVarrs796052943
Maprs796052943
PheGenIrs796052943
Biobankrs796052943
1000 genomesrs796052943
hgdprs796052943
ensemblrs796052943
geneviewrs796052943
scholarrs796052943
googlers796052943
pharmgkbrs796052943
gwascentralrs796052943
openSNPrs796052943
23andMers796052943
SNPshotrs796052943
SNPdbers796052943
MSV3drs796052943
GWAS Ctlgrs796052943
Max Magnitude0
ClinVar
Risk rs796052943(-;-)
Alt rs796052943(-;-)
Reference Rs796052943(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC100289283 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824590_29824591delCA
CLNSRC
CLNACC RCV000188784.1,