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rs587777258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777258(-;-)
Make rs587777258(-;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position91146176
GeneDCN
is asnp
is mentioned by
dbSNPrs587777258
ebirs587777258
HLIrs587777258
Exacrs587777258
Varsomers587777258
Maprs587777258
PheGenIrs587777258
hapmaprs587777258
1000 genomesrs587777258
hgdprs587777258
ensemblrs587777258
gopubmedrs587777258
geneviewrs587777258
scholarrs587777258
googlers587777258
pharmgkbrs587777258
gwascentralrs587777258
openSNPrs587777258
23andMers587777258
23andMe allrs587777258
SNP Nexus

SNPshotrs587777258
SNPdbers587777258
MSV3drs587777258
GWAS Ctlgrs587777258
Max Magnitude0
ClinVar
Risk rs587777258(TG,G;TG,G)
Alt rs587777258(TG,G;TG,G)
Reference rs587777258(AG;AG)
Significance Pathogenic
Disease Congenital Stromal Corneal Dystrophy
Variation info
Gene DCN
CLNDBN Congenital Stromal Corneal Dystrophy
Reversed 1
HGVS NC_000012.11:g.91539953delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000114315.3,