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rs121917862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917862(A;A)
Make rs121917862(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position91055638
GeneKERA
is asnp
is mentioned by
dbSNPrs121917862
ebirs121917862
HLIrs121917862
Exacrs121917862
Varsomers121917862
Maprs121917862
PheGenIrs121917862
hapmaprs121917862
1000 genomesrs121917862
hgdprs121917862
ensemblrs121917862
gopubmedrs121917862
geneviewrs121917862
scholarrs121917862
googlers121917862
pharmgkbrs121917862
gwascentralrs121917862
openSNPrs121917862
23andMers121917862
23andMe allrs121917862
SNP Nexus

SNPshotrs121917862
SNPdbers121917862
MSV3drs121917862
GWAS Ctlgrs121917862
Max Magnitude0
ClinVar
Risk rs121917862(A;A)
Alt rs121917862(A;A)
Reference rs121917862(C;C)
Significance Pathogenic
Disease Cornea plana 2
Variation info
Gene KERA
CLNDBN Cornea plana 2
Reversed 1
HGVS NC_000012.11:g.91449415G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006894.2,