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rs397514638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514638(C;C)
Make rs397514638(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position74181301
GeneSTRA6
is asnp
is mentioned by
dbSNPrs397514638
ebirs397514638
HLIrs397514638
Exacrs397514638
Varsomers397514638
Maprs397514638
PheGenIrs397514638
hapmaprs397514638
1000 genomesrs397514638
hgdprs397514638
ensemblrs397514638
gopubmedrs397514638
geneviewrs397514638
scholarrs397514638
googlers397514638
pharmgkbrs397514638
gwascentralrs397514638
openSNPrs397514638
23andMers397514638
23andMe allrs397514638
SNP Nexus

SNPshotrs397514638
SNPdbers397514638
MSV3drs397514638
GWAS Ctlgrs397514638
Max Magnitude0
ClinVar
Risk rs397514638(A,C;A,C)
Alt rs397514638(A,C;A,C)
Reference rs397514638(G;G)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74473642C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000033165.2,