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rs387906901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906901(A;A)
Make rs387906901(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position193667191
GeneOPA1
is asnp
is mentioned by
dbSNPrs387906901
ebirs387906901
HLIrs387906901
Exacrs387906901
Varsomers387906901
Maprs387906901
PheGenIrs387906901
hapmaprs387906901
1000 genomesrs387906901
hgdprs387906901
ensemblrs387906901
gopubmedrs387906901
geneviewrs387906901
scholarrs387906901
googlers387906901
pharmgkbrs387906901
gwascentralrs387906901
openSNPrs387906901
23andMers387906901
23andMe allrs387906901
SNP Nexus

SNPshotrs387906901
SNPdbers387906901
MSV3drs387906901
GWAS Ctlgrs387906901
Max Magnitude0
ClinVar
Risk rs387906901(A;A)
Alt rs387906901(A;A)
Reference rs387906901(T;T)
Significance Pathogenic
Disease Optic Atrophy Type 1
Variation info
Gene OPA1 LOC101929213
CLNDBN Optic Atrophy Type 1
Reversed 0
HGVS NC_000003.11:g.193384980T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023417.3,