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rs387907252

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907252(A;A)
Make rs387907252(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position117134559
GeneVAX1
is asnp
is mentioned by
dbSNPrs387907252
ebirs387907252
HLIrs387907252
Exacrs387907252
Varsomers387907252
Maprs387907252
PheGenIrs387907252
hapmaprs387907252
1000 genomesrs387907252
hgdprs387907252
ensemblrs387907252
gopubmedrs387907252
geneviewrs387907252
scholarrs387907252
googlers387907252
pharmgkbrs387907252
gwascentralrs387907252
openSNPrs387907252
23andMers387907252
23andMe allrs387907252
SNP Nexus

SNPshotrs387907252
SNPdbers387907252
MSV3drs387907252
GWAS Ctlgrs387907252
Max Magnitude0
ClinVar
Risk rs387907252(A;A)
Alt rs387907252(A;A)
Reference rs387907252(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene VAX1
CLNDBN Microphthalmia, syndromic 11
Reversed 1
HGVS NC_000010.10:g.118894070G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030635.3,