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rs397515545

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515545(-;-)
Make rs397515545(-;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position91146191
GeneDCN
is asnp
is mentioned by
dbSNPrs397515545
ebirs397515545
HLIrs397515545
Exacrs397515545
Varsomers397515545
Maprs397515545
PheGenIrs397515545
hapmaprs397515545
1000 genomesrs397515545
hgdprs397515545
ensemblrs397515545
gopubmedrs397515545
geneviewrs397515545
scholarrs397515545
googlers397515545
pharmgkbrs397515545
gwascentralrs397515545
openSNPrs397515545
23andMers397515545
23andMe allrs397515545
SNP Nexus

SNPshotrs397515545
SNPdbers397515545
MSV3drs397515545
GWAS Ctlgrs397515545
Max Magnitude0
ClinVar
Risk rs397515545(;)
Alt rs397515545(;)
Reference rs397515545(G;G)
Significance Pathogenic
Disease Congenital Stromal Corneal Dystrophy
Variation info
Gene DCN
CLNDBN Congenital Stromal Corneal Dystrophy
Reversed 1
HGVS NC_000012.11:g.91539968delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000055876.5,