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rs193302994

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193302994(A;A)
Make rs193302994(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15452
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302994
ebirs193302994
HLIrs193302994
Exacrs193302994
Varsomers193302994
Maprs193302994
PheGenIrs193302994
hapmaprs193302994
1000 genomesrs193302994
hgdprs193302994
ensemblrs193302994
gopubmedrs193302994
geneviewrs193302994
scholarrs193302994
googlers193302994
pharmgkbrs193302994
gwascentralrs193302994
openSNPrs193302994
23andMers193302994
23andMe allrs193302994
SNP Nexus

SNPshotrs193302994
SNPdbers193302994
MSV3drs193302994
GWAS Ctlgrs193302994
Max Magnitude0
ClinVar
Risk rs193302994(A,T;A,T)
Alt rs193302994(A,T;A,T)
Reference rs193302994(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15452C>A
CLNSRC
CLNACC RCV000133456.1,