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

rs193302980

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193302980(C;C)
Make rs193302980(C;T)
Make rs193302980(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14766
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302980
ebirs193302980
HLIrs193302980
Exacrs193302980
Varsomers193302980
Maprs193302980
PheGenIrs193302980
hapmaprs193302980
1000 genomesrs193302980
hgdprs193302980
ensemblrs193302980
gopubmedrs193302980
geneviewrs193302980
scholarrs193302980
googlers193302980
pharmgkbrs193302980
gwascentralrs193302980
openSNPrs193302980
23andMers193302980
23andMe allrs193302980
SNP Nexus

SNPshotrs193302980
SNPdbers193302980
MSV3drs193302980
GWAS Ctlgrs193302980
Max Magnitude0
ClinVar
Risk rs193302980(A;A)
Alt rs193302980(A;A)
Reference rs193302980(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.14766C>T
CLNSRC
CLNACC RCV000128802.1,