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

rs193302983

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193302983(A;A)
Make rs193302983(A;G)
Make rs193302983(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14905
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302983
ebirs193302983
HLIrs193302983
Exacrs193302983
Varsomers193302983
Maprs193302983
PheGenIrs193302983
hapmaprs193302983
1000 genomesrs193302983
hgdprs193302983
ensemblrs193302983
gopubmedrs193302983
geneviewrs193302983
scholarrs193302983
googlers193302983
pharmgkbrs193302983
gwascentralrs193302983
openSNPrs193302983
23andMers193302983
23andMe allrs193302983
SNP Nexus

SNPshotrs193302983
SNPdbers193302983
MSV3drs193302983
GWAS Ctlgrs193302983
Max Magnitude0
ClinVar
Risk rs193302983(T;T)
Alt rs193302983(T;T)
Reference rs193302983(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_012920.1:m.14905G>A
CLNSRC
CLNACC RCV000133450.1,