Have questions? Visit https://www.reddit.com/r/SNPedia

rs193302982

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193302982(C;C)
Make rs193302982(C;T)
Make rs193302982(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14783
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302982
ebirs193302982
HLIrs193302982
Exacrs193302982
Varsomers193302982
Maprs193302982
PheGenIrs193302982
hapmaprs193302982
1000 genomesrs193302982
hgdprs193302982
ensemblrs193302982
gopubmedrs193302982
geneviewrs193302982
scholarrs193302982
googlers193302982
pharmgkbrs193302982
gwascentralrs193302982
openSNPrs193302982
23andMers193302982
23andMe allrs193302982
SNP Nexus

SNPshotrs193302982
SNPdbers193302982
MSV3drs193302982
GWAS Ctlgrs193302982
Max Magnitude0
ClinVar
Risk rs193302982(G;G)
Alt rs193302982(G;G)
Reference rs193302982(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_012920.1:m.14783T>C
CLNSRC
CLNACC RCV000128803.1,