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rs794728075

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728075(C;G)
Make rs794728075(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31082378
GeneDSC2
is asnp
is mentioned by
dbSNPrs794728075
ebirs794728075
HLIrs794728075
Exacrs794728075
Varsomers794728075
Maprs794728075
PheGenIrs794728075
hapmaprs794728075
1000 genomesrs794728075
hgdprs794728075
ensemblrs794728075
gopubmedrs794728075
geneviewrs794728075
scholarrs794728075
googlers794728075
pharmgkbrs794728075
gwascentralrs794728075
openSNPrs794728075
23andMers794728075
23andMe allrs794728075
SNP Nexus

SNPshotrs794728075
SNPdbers794728075
MSV3drs794728075
GWAS Ctlgrs794728075
Max Magnitude0
ClinVar
Risk rs794728075(G;G)
Alt rs794728075(G;G)
Reference rs794728075(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.28662344G>C
CLNSRC
CLNACC RCV000181177.1,