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rs193302993

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193302993(A;A)
Make rs193302993(A;G)
Make rs193302993(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15431
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302993
ebirs193302993
HLIrs193302993
Exacrs193302993
Varsomers193302993
Maprs193302993
PheGenIrs193302993
hapmaprs193302993
1000 genomesrs193302993
hgdprs193302993
ensemblrs193302993
gopubmedrs193302993
geneviewrs193302993
scholarrs193302993
googlers193302993
pharmgkbrs193302993
gwascentralrs193302993
openSNPrs193302993
23andMers193302993
23andMe allrs193302993
SNP Nexus

SNPshotrs193302993
SNPdbers193302993
MSV3drs193302993
GWAS Ctlgrs193302993
Max Magnitude0
ClinVar
Risk rs193302993(T;T)
Alt rs193302993(T;T)
Reference rs193302993(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 1
HGVS NC_012920.1:m.15431G>A
CLNSRC
CLNACC RCV000133455.1,