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rs762556795

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762556795(C;T)
Make rs762556795(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31101968
GeneDSCAS, DSC2
is asnp
is mentioned by
dbSNPrs762556795
ebirs762556795
HLIrs762556795
Exacrs762556795
Varsomers762556795
Maprs762556795
PheGenIrs762556795
hapmaprs762556795
1000 genomesrs762556795
hgdprs762556795
ensemblrs762556795
gopubmedrs762556795
geneviewrs762556795
scholarrs762556795
googlers762556795
pharmgkbrs762556795
gwascentralrs762556795
openSNPrs762556795
23andMers762556795
23andMe allrs762556795
SNP Nexus

SNPshotrs762556795
SNPdbers762556795
MSV3drs762556795
GWAS Ctlgrs762556795
Max Magnitude0
ClinVar
Risk rs762556795(T;T)
Alt rs762556795(T;T)
Reference rs762556795(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DSC2 DSCAS LOC101927698
CLNDBN not specified
Reversed 0
HGVS NC_000018.9:g.28681931C>T
CLNSRC
CLNACC RCV000181170.2,