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rs527236168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236168(C;G)
Make rs527236168(G;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position14974
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs527236168
ebirs527236168
HLIrs527236168
Exacrs527236168
Varsomers527236168
Maprs527236168
PheGenIrs527236168
hapmaprs527236168
1000 genomesrs527236168
hgdprs527236168
ensemblrs527236168
gopubmedrs527236168
geneviewrs527236168
scholarrs527236168
googlers527236168
pharmgkbrs527236168
gwascentralrs527236168
openSNPrs527236168
23andMers527236168
23andMe allrs527236168
SNP Nexus

SNPshotrs527236168
SNPdbers527236168
MSV3drs527236168
GWAS Ctlgrs527236168
Max Magnitude0
ClinVar
Risk rs527236168(G,T;G,T)
Alt rs527236168(G,T;G,T)
Reference rs527236168(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.14974C>G
CLNSRC ClinVar
CLNACC RCV000133410.1,