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rs869025268

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025268(-;-)
Make rs869025268(-;G)
Make rs869025268(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position74239632
GeneVSX2
is asnp
is mentioned by
dbSNPrs869025268
ebirs869025268
HLIrs869025268
Exacrs869025268
Varsomers869025268
Maprs869025268
PheGenIrs869025268
hapmaprs869025268
1000 genomesrs869025268
hgdprs869025268
ensemblrs869025268
gopubmedrs869025268
geneviewrs869025268
scholarrs869025268
googlers869025268
pharmgkbrs869025268
gwascentralrs869025268
openSNPrs869025268
23andMers869025268
23andMe allrs869025268
SNP Nexus

SNPshotrs869025268
SNPdbers869025268
MSV3drs869025268
GWAS Ctlgrs869025268
Max Magnitude0
ClinVar
Risk rs869025268(G;G)
Alt rs869025268(G;G)
Reference rs869025268(;)
Significance Pathogenic
Disease Anophthalmia - microphthalmia
Variation info
Gene VSX2
CLNDBN Anophthalmia - microphthalmia
Reversed 0
HGVS NC_000014.8:g.74706335dupG
CLNSRC
CLNACC RCV000207414.1,