Have questions? Visit https://www.reddit.com/r/SNPedia

rs397518484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397518484(A;A)
Make rs397518484(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position74181459
GeneSTRA6
is asnp
is mentioned by
dbSNPrs397518484
ebirs397518484
HLIrs397518484
Exacrs397518484
Varsomers397518484
Maprs397518484
PheGenIrs397518484
hapmaprs397518484
1000 genomesrs397518484
hgdprs397518484
ensemblrs397518484
gopubmedrs397518484
geneviewrs397518484
scholarrs397518484
googlers397518484
pharmgkbrs397518484
gwascentralrs397518484
openSNPrs397518484
23andMers397518484
23andMe allrs397518484
SNP Nexus

SNPshotrs397518484
SNPdbers397518484
MSV3drs397518484
GWAS Ctlgrs397518484
Max Magnitude0
ClinVar
Risk rs397518484(A;A)
Alt rs397518484(A;A)
Reference rs397518484(G;G)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74473800C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074414.2,