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rs74315434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs74315434(A;A)
Make rs74315434(A;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position25079464
GeneVSX1
is asnp
is mentioned by
dbSNPrs74315434
ebirs74315434
HLIrs74315434
Exacrs74315434
Varsomers74315434
Maprs74315434
PheGenIrs74315434
hapmaprs74315434
1000 genomesrs74315434
hgdprs74315434
ensemblrs74315434
gopubmedrs74315434
geneviewrs74315434
scholarrs74315434
googlers74315434
pharmgkbrs74315434
gwascentralrs74315434
openSNPrs74315434
23andMers74315434
23andMe allrs74315434
SNP Nexus

SNPshotrs74315434
SNPdbers74315434
MSV3drs74315434
GWAS Ctlgrs74315434
Max Magnitude0
OMIM605020
Desc
Variant0003
Relatedalso
ClinVar
Risk rs74315434(A;A)
Alt rs74315434(A;A)
Reference rs74315434(T;T)
Significance Unknown
Disease Keratoconus 1
Variation info
Gene VSX1
CLNDBN Keratoconus 1
Reversed 1
HGVS NC_000020.10:g.25060100A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005561.3,