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rs41518645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41518645(A;A)
Make rs41518645(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15257
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs41518645
ebirs41518645
HLIrs41518645
Exacrs41518645
Varsomers41518645
Maprs41518645
PheGenIrs41518645
hapmaprs41518645
1000 genomesrs41518645
hgdprs41518645
ensemblrs41518645
gopubmedrs41518645
geneviewrs41518645
scholarrs41518645
googlers41518645
pharmgkbrs41518645
gwascentralrs41518645
openSNPrs41518645
23andMers41518645
23andMe allrs41518645
SNP Nexus

SNPshotrs41518645
SNPdbers41518645
MSV3drs41518645
GWAS Ctlgrs41518645
GMAF0.006548
Max Magnitude0
ClinVar
Risk rs41518645(A;A)
Alt rs41518645(A;A)
Reference rs41518645(G;G)
Significance Other
Disease Leber's optic atrophy
Variation info
Gene CYTB
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.15257G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010312.4,