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rs794728076

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728076(A;A)
Make rs794728076(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31080340
GeneDSC2
is asnp
is mentioned by
dbSNPrs794728076
ebirs794728076
HLIrs794728076
Exacrs794728076
Varsomers794728076
Maprs794728076
PheGenIrs794728076
hapmaprs794728076
1000 genomesrs794728076
hgdprs794728076
ensemblrs794728076
gopubmedrs794728076
geneviewrs794728076
scholarrs794728076
googlers794728076
pharmgkbrs794728076
gwascentralrs794728076
openSNPrs794728076
23andMers794728076
23andMe allrs794728076
SNP Nexus

SNPshotrs794728076
SNPdbers794728076
MSV3drs794728076
GWAS Ctlgrs794728076
Max Magnitude0
ClinVar
Risk rs794728076(A;A)
Alt rs794728076(A;A)
Reference rs794728076(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DSC2
CLNDBN not specified
Reversed 1
HGVS NC_000018.9:g.28660306C>T
CLNSRC
CLNACC RCV000181178.2,