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rs193302997

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193302997(C;C)
Make rs193302997(C;T)
Make rs193302997(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15670
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302997
ebirs193302997
HLIrs193302997
Exacrs193302997
Varsomers193302997
Maprs193302997
PheGenIrs193302997
hapmaprs193302997
1000 genomesrs193302997
hgdprs193302997
ensemblrs193302997
gopubmedrs193302997
geneviewrs193302997
scholarrs193302997
googlers193302997
pharmgkbrs193302997
gwascentralrs193302997
openSNPrs193302997
23andMers193302997
23andMe allrs193302997
SNP Nexus

SNPshotrs193302997
SNPdbers193302997
MSV3drs193302997
GWAS Ctlgrs193302997
Max Magnitude0
ClinVar
Risk rs193302997(G;G)
Alt rs193302997(G;G)
Reference rs193302997(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 1
HGVS NC_012920.1:m.15670T>C
CLNSRC
CLNACC RCV000133458.1,