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rs397515639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515639(C;T)
Make rs397515639(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31326608
GeneDSG1
is asnp
is mentioned by
dbSNPrs397515639
ebirs397515639
HLIrs397515639
Exacrs397515639
Varsomers397515639
Maprs397515639
PheGenIrs397515639
hapmaprs397515639
1000 genomesrs397515639
hgdprs397515639
ensemblrs397515639
gopubmedrs397515639
geneviewrs397515639
scholarrs397515639
googlers397515639
pharmgkbrs397515639
gwascentralrs397515639
openSNPrs397515639
23andMers397515639
23andMe allrs397515639
SNP Nexus

SNPshotrs397515639
SNPdbers397515639
MSV3drs397515639
GWAS Ctlgrs397515639
Max Magnitude0
ClinVar
Risk rs397515639(T;T)
Alt rs397515639(T;T)
Reference rs397515639(C;C)
Significance Pathogenic
Disease Keratosis palmoplantaris striata 1
Variation info
Gene DSG1
CLNDBN Keratosis palmoplantaris striata 1
Reversed 0
HGVS NC_000018.9:g.28906571C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074351.2,