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rs74315432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 4 keratoconus
Make rs74315432(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position25079443
GeneVSX1
is asnp
is mentioned by
dbSNPrs74315432
ebirs74315432
HLIrs74315432
Exacrs74315432
Varsomers74315432
Maprs74315432
PheGenIrs74315432
hapmaprs74315432
1000 genomesrs74315432
hgdprs74315432
ensemblrs74315432
gopubmedrs74315432
geneviewrs74315432
scholarrs74315432
googlers74315432
pharmgkbrs74315432
gwascentralrs74315432
openSNPrs74315432
23andMers74315432
23andMe allrs74315432
SNP Nexus

SNPshotrs74315432
SNPdbers74315432
MSV3drs74315432
GWAS Ctlgrs74315432
Max Magnitude4
OMIM605020
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315432(A,T;A,T)
Alt rs74315432(A,T;A,T)
Reference rs74315432(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene VSX1
CLNDBN Keratoconus 1
Reversed 1
HGVS NC_000020.10:g.25060079G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005559.2,