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rs527236192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236192(A;G)
Make rs527236192(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15682
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236192
ebirs527236192
HLIrs527236192
Exacrs527236192
Varsomers527236192
Maprs527236192
PheGenIrs527236192
hapmaprs527236192
1000 genomesrs527236192
hgdprs527236192
ensemblrs527236192
gopubmedrs527236192
geneviewrs527236192
scholarrs527236192
googlers527236192
pharmgkbrs527236192
gwascentralrs527236192
openSNPrs527236192
23andMers527236192
23andMe allrs527236192
SNP Nexus

SNPshotrs527236192
SNPdbers527236192
MSV3drs527236192
GWAS Ctlgrs527236192
Max Magnitude0
ClinVar
Risk rs527236192(G;G)
Alt rs527236192(G;G)
Reference rs527236192(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15682A>G
CLNSRC ClinVar
CLNACC RCV000133436.1,