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rs386419981

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386419981(A;A)
Make rs386419981(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position14891
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs386419981
ebirs386419981
HLIrs386419981
Exacrs386419981
Varsomers386419981
Maprs386419981
PheGenIrs386419981
hapmaprs386419981
1000 genomesrs386419981
hgdprs386419981
ensemblrs386419981
gopubmedrs386419981
geneviewrs386419981
scholarrs386419981
googlers386419981
pharmgkbrs386419981
gwascentralrs386419981
openSNPrs386419981
23andMers386419981
23andMe allrs386419981
SNP Nexus

SNPshotrs386419981
SNPdbers386419981
MSV3drs386419981
GWAS Ctlgrs386419981
Merged fromRs527236165
Max Magnitude0
ClinVar
Risk rs386419981(C;C)
Alt rs386419981(C;C)
Reference rs386419981(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_012920.1:m.14891C>G
CLNSRC
CLNACC RCV000133407.1,