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rs193302996

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193302996(A;G)
Make rs193302996(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15607
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302996
ebirs193302996
HLIrs193302996
Exacrs193302996
Varsomers193302996
Maprs193302996
PheGenIrs193302996
hapmaprs193302996
1000 genomesrs193302996
hgdprs193302996
ensemblrs193302996
gopubmedrs193302996
geneviewrs193302996
scholarrs193302996
googlers193302996
pharmgkbrs193302996
gwascentralrs193302996
openSNPrs193302996
23andMers193302996
23andMe allrs193302996
SNP Nexus

SNPshotrs193302996
SNPdbers193302996
MSV3drs193302996
GWAS Ctlgrs193302996
Max Magnitude0
ClinVar
Risk rs193302996(G;G)
Alt rs193302996(G;G)
Reference rs193302996(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15607A>G
CLNSRC
CLNACC RCV000133457.1,