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rs758527425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758527425(C;T)
Make rs758527425(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position31089461
GeneDSC2
is asnp
is mentioned by
dbSNPrs758527425
dbSNP (classic)rs758527425
ClinGenrs758527425
ebirs758527425
HLIrs758527425
Exacrs758527425
Gnomadrs758527425
Varsomers758527425
LitVarrs758527425
Maprs758527425
PheGenIrs758527425
Biobankrs758527425
1000 genomesrs758527425
hgdprs758527425
ensemblrs758527425
geneviewrs758527425
scholarrs758527425
googlers758527425
pharmgkbrs758527425
gwascentralrs758527425
openSNPrs758527425
23andMers758527425
SNPshotrs758527425
SNPdbers758527425
MSV3drs758527425
GWAS Ctlgrs758527425
Max Magnitude0
ClinVar
Risk rs758527425(T;T)
Alt rs758527425(T;T)
Reference Rs758527425(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.28669424C>T
CLNSRC
CLNACC RCV000413449.1,