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rs794728072

From SNPedia

Orientationminus
Make rs794728072(-;-)
Make rs794728072(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31071604
GeneDSC2
is asnp
is mentioned by
dbSNPrs794728072
ebirs794728072
HLIrs794728072
Exacrs794728072
Varsomers794728072
Maprs794728072
PheGenIrs794728072
hapmaprs794728072
1000 genomesrs794728072
hgdprs794728072
ensemblrs794728072
gopubmedrs794728072
geneviewrs794728072
scholarrs794728072
googlers794728072
pharmgkbrs794728072
gwascentralrs794728072
openSNPrs794728072
23andMers794728072
23andMe allrs794728072
SNP Nexus

SNPshotrs794728072
SNPdbers794728072
MSV3drs794728072
GWAS Ctlgrs794728072
Max Magnitude
ClinVar
Risk
Alt
Reference Rs794728072(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.28651570delC
CLNSRC
CLNACC RCV000181172.2,