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rs121917858

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121917858(A;G)
Make rs121917858(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position91055542
GeneKERA
is asnp
is mentioned by
dbSNPrs121917858
ebirs121917858
HLIrs121917858
Exacrs121917858
Varsomers121917858
Maprs121917858
PheGenIrs121917858
hapmaprs121917858
1000 genomesrs121917858
hgdprs121917858
ensemblrs121917858
gopubmedrs121917858
geneviewrs121917858
scholarrs121917858
googlers121917858
pharmgkbrs121917858
gwascentralrs121917858
openSNPrs121917858
23andMers121917858
23andMe allrs121917858
SNP Nexus

SNPshotrs121917858
SNPdbers121917858
MSV3drs121917858
GWAS Ctlgrs121917858
Max Magnitude0
ClinVar
Risk rs121917858(G;G)
Alt rs121917858(G;G)
Reference rs121917858(A;A)
Significance Pathogenic
Disease Cornea plana 2
Variation info
Gene KERA
CLNDBN Cornea plana 2
Reversed 1
HGVS NC_000012.11:g.91449319T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006892.2,