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rs869025269

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025269(A;G)
Make rs869025269(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position74182448
GeneSTRA6
is asnp
is mentioned by
dbSNPrs869025269
ebirs869025269
HLIrs869025269
Exacrs869025269
Varsomers869025269
Maprs869025269
PheGenIrs869025269
hapmaprs869025269
1000 genomesrs869025269
hgdprs869025269
ensemblrs869025269
gopubmedrs869025269
geneviewrs869025269
scholarrs869025269
googlers869025269
pharmgkbrs869025269
gwascentralrs869025269
openSNPrs869025269
23andMers869025269
23andMe allrs869025269
SNP Nexus

SNPshotrs869025269
SNPdbers869025269
MSV3drs869025269
GWAS Ctlgrs869025269
Max Magnitude0
ClinVar
Risk rs869025269(G;G)
Alt rs869025269(G;G)
Reference rs869025269(A;A)
Significance Pathogenic
Disease Anophthalmia - microphthalmia
Variation info
Gene STRA6
CLNDBN Anophthalmia - microphthalmia
Reversed 1
HGVS NC_000015.9:g.74474789T>C
CLNSRC
CLNACC RCV000207353.1,