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rs193302985

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193302985(A;A)
Make rs193302985(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15043
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302985
ebirs193302985
HLIrs193302985
Exacrs193302985
Varsomers193302985
Maprs193302985
PheGenIrs193302985
hapmaprs193302985
1000 genomesrs193302985
hgdprs193302985
ensemblrs193302985
gopubmedrs193302985
geneviewrs193302985
scholarrs193302985
googlers193302985
pharmgkbrs193302985
gwascentralrs193302985
openSNPrs193302985
23andMers193302985
23andMe allrs193302985
SNP Nexus

SNPshotrs193302985
SNPdbers193302985
MSV3drs193302985
GWAS Ctlgrs193302985
Max Magnitude0
ClinVar
Risk rs193302985(A;A)
Alt rs193302985(A;A)
Reference rs193302985(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15043G>A
CLNSRC
CLNACC RCV000128804.1,