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rs397514639

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514639(A;A)
Make rs397514639(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position74180120
GeneSTRA6
is asnp
is mentioned by
dbSNPrs397514639
ebirs397514639
HLIrs397514639
Exacrs397514639
Varsomers397514639
Maprs397514639
PheGenIrs397514639
hapmaprs397514639
1000 genomesrs397514639
hgdprs397514639
ensemblrs397514639
gopubmedrs397514639
geneviewrs397514639
scholarrs397514639
googlers397514639
pharmgkbrs397514639
gwascentralrs397514639
openSNPrs397514639
23andMers397514639
23andMe allrs397514639
SNP Nexus

SNPshotrs397514639
SNPdbers397514639
MSV3drs397514639
GWAS Ctlgrs397514639
Max Magnitude0
ClinVar
Risk rs397514639(A;A)
Alt rs397514639(A;A)
Reference rs397514639(G;G)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74472461C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033166.3,