Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728073

From SNPedia

Orientationminus
Make rs794728073(-;-)
Make rs794728073(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31068915
GeneDSC2
is asnp
is mentioned by
dbSNPrs794728073
ebirs794728073
HLIrs794728073
Exacrs794728073
Varsomers794728073
Maprs794728073
PheGenIrs794728073
hapmaprs794728073
1000 genomesrs794728073
hgdprs794728073
ensemblrs794728073
gopubmedrs794728073
geneviewrs794728073
scholarrs794728073
googlers794728073
pharmgkbrs794728073
gwascentralrs794728073
openSNPrs794728073
23andMers794728073
23andMe allrs794728073
SNP Nexus

SNPshotrs794728073
SNPdbers794728073
MSV3drs794728073
GWAS Ctlgrs794728073
Max Magnitude
ClinVar
Risk rs794728073(;)
Alt rs794728073(;)
Reference rs794728073(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.28648881delA
CLNSRC
CLNACC RCV000181174.1,