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rs527236174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236174(A;G)
Make rs527236174(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position15226
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236174
ebirs527236174
HLIrs527236174
Exacrs527236174
Varsomers527236174
Maprs527236174
PheGenIrs527236174
hapmaprs527236174
1000 genomesrs527236174
hgdprs527236174
ensemblrs527236174
gopubmedrs527236174
geneviewrs527236174
scholarrs527236174
googlers527236174
pharmgkbrs527236174
gwascentralrs527236174
openSNPrs527236174
23andMers527236174
23andMe allrs527236174
SNP Nexus

SNPshotrs527236174
SNPdbers527236174
MSV3drs527236174
GWAS Ctlgrs527236174
Max Magnitude0
ClinVar
Risk rs527236174(G;G)
Alt rs527236174(G;G)
Reference rs527236174(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.15226A>G
CLNSRC ClinVar
CLNACC RCV000133416.1,