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rs606231125

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231125(-;-)
Make rs606231125(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position74197785
GeneSTRA6
is asnp
is mentioned by
dbSNPrs606231125
ebirs606231125
HLIrs606231125
Exacrs606231125
Varsomers606231125
Maprs606231125
PheGenIrs606231125
hapmaprs606231125
1000 genomesrs606231125
hgdprs606231125
ensemblrs606231125
gopubmedrs606231125
geneviewrs606231125
scholarrs606231125
googlers606231125
pharmgkbrs606231125
gwascentralrs606231125
openSNPrs606231125
23andMers606231125
23andMe allrs606231125
SNP Nexus

SNPshotrs606231125
SNPdbers606231125
MSV3drs606231125
GWAS Ctlgrs606231125
Max Magnitude0
ClinVar
Risk rs606231125(;)
Alt rs606231125(;)
Reference rs606231125(C;C)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74490126delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000001193.4,