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rs796065303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065303(-;-)
Make rs796065303(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position823744
GeneCRACR2B, PNPLA2
is asnp
is mentioned by
dbSNPrs796065303
dbSNP (old)rs796065303
ClinGenrs796065303
ebirs796065303
HLIrs796065303
Exacrs796065303
Gnomadrs796065303
Varsomers796065303
Maprs796065303
PheGenIrs796065303
Biobankrs796065303
1000 genomesrs796065303
hgdprs796065303
ensemblrs796065303
gopubmedrs796065303
geneviewrs796065303
scholarrs796065303
googlers796065303
pharmgkbrs796065303
gwascentralrs796065303
openSNPrs796065303
23andMers796065303
23andMe allrs796065303
SNP Nexus

SNPshotrs796065303
SNPdbers796065303
MSV3drs796065303
GWAS Ctlgrs796065303
Max Magnitude0
ClinVar
Risk rs796065303(-;-)
Alt rs796065303(-;-)
Reference Rs796065303(C;C)
Significance Pathogenic
Disease Neutral lipid storage disease with myopathy
Variation info
Gene PNPLA2 RPLP2
CLNDBN Neutral lipid storage disease with myopathy
Reversed 0
HGVS NC_000011.9:g.823744delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001950.2,