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rs796052944

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052944(-;C)
Make rs796052944(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position29813487
GenePRRT2
is asnp
is mentioned by
dbSNPrs796052944
ClinGenrs796052944
ebirs796052944
HLIrs796052944
Exacrs796052944
Varsomers796052944
Maprs796052944
PheGenIrs796052944
hapmaprs796052944
1000 genomesrs796052944
hgdprs796052944
ensemblrs796052944
gopubmedrs796052944
geneviewrs796052944
scholarrs796052944
googlers796052944
pharmgkbrs796052944
gwascentralrs796052944
openSNPrs796052944
23andMers796052944
23andMe allrs796052944
SNP Nexus

SNPshotrs796052944
SNPdbers796052944
MSV3drs796052944
GWAS Ctlgrs796052944
Max Magnitude0
ClinVar
Risk rs796052944(C;C)
Alt rs796052944(C;C)
Reference Rs796052944(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC100289283 PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824808dupC
CLNSRC
CLNACC RCV000188785.1,