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rs387906899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906899(A;G)
Make rs387906899(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position193643609
GeneOPA1
is asnp
is mentioned by
dbSNPrs387906899
ebirs387906899
HLIrs387906899
Exacrs387906899
Varsomers387906899
Maprs387906899
PheGenIrs387906899
hapmaprs387906899
1000 genomesrs387906899
hgdprs387906899
ensemblrs387906899
gopubmedrs387906899
geneviewrs387906899
scholarrs387906899
googlers387906899
pharmgkbrs387906899
gwascentralrs387906899
openSNPrs387906899
23andMers387906899
23andMe allrs387906899
SNP Nexus

SNPshotrs387906899
SNPdbers387906899
MSV3drs387906899
GWAS Ctlgrs387906899
Max Magnitude0
ClinVar
Risk rs387906899(G;G)
Alt rs387906899(G;G)
Reference rs387906899(A;A)
Significance Pathogenic
Disease Optic Atrophy Type 1
Variation info
Gene OPA1
CLNDBN Optic Atrophy Type 1
Reversed 0
HGVS NC_000003.11:g.193361398A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023414.2,