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rs60410063

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs60410063(G;T)
Make rs60410063(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position52791233
GeneKRT3
is asnp
is mentioned by
dbSNPrs60410063
ebirs60410063
HLIrs60410063
Exacrs60410063
Varsomers60410063
Maprs60410063
PheGenIrs60410063
hapmaprs60410063
1000 genomesrs60410063
hgdprs60410063
ensemblrs60410063
gopubmedrs60410063
geneviewrs60410063
scholarrs60410063
googlers60410063
pharmgkbrs60410063
gwascentralrs60410063
openSNPrs60410063
23andMers60410063
23andMe allrs60410063
SNP Nexus

SNPshotrs60410063
SNPdbers60410063
MSV3drs60410063
GWAS Ctlgrs60410063
Max Magnitude0


ClinVar
Risk rs60410063(A,C,T;A,C,T)
Alt rs60410063(A,C,T;A,C,T)
Reference rs60410063(G;G)
Significance Pathogenic
Disease not provided Meesman's corneal dystrophy
Variation info
Gene KRT3
CLNDBN not provided Meesman's corneal dystrophy
Reversed 1
HGVS NC_000012.11:g.53185017C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000057203.1, RCV000118978.3,