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rs267607096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607096(A;A)
Make rs267607096(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position74202199
GeneSTRA6
is asnp
is mentioned by
dbSNPrs267607096
ebirs267607096
HLIrs267607096
Exacrs267607096
Varsomers267607096
Maprs267607096
PheGenIrs267607096
hapmaprs267607096
1000 genomesrs267607096
hgdprs267607096
ensemblrs267607096
gopubmedrs267607096
geneviewrs267607096
scholarrs267607096
googlers267607096
pharmgkbrs267607096
gwascentralrs267607096
openSNPrs267607096
23andMers267607096
23andMe allrs267607096
SNP Nexus

SNPshotrs267607096
SNPdbers267607096
MSV3drs267607096
GWAS Ctlgrs267607096
Max Magnitude0
ClinVar
Risk rs267607096(A;A)
Alt rs267607096(A;A)
Reference rs267607096(G;G)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74494540C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001201.3,