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rs527236210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236210(A;G)
Make rs527236210(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15607
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236210
dbSNP (classic)rs527236210
ClinGenrs527236210
ebirs527236210
HLIrs527236210
Exacrs527236210
Gnomadrs527236210
Varsomers527236210
LitVarrs527236210
Maprs527236210
PheGenIrs527236210
Biobankrs527236210
1000 genomesrs527236210
hgdprs527236210
ensemblrs527236210
geneviewrs527236210
scholarrs527236210
googlers527236210
pharmgkbrs527236210
gwascentralrs527236210
openSNPrs527236210
23andMers527236210
SNPshotrs527236210
SNPdbers527236210
MSV3drs527236210
GWAS Ctlgrs527236210
Merged fromRs28357372
Max Magnitude0
? (A;A) (A;G) (G;G) 28


ClinVar
Risk rs527236210(G;G)
Alt rs527236210(G;G)
Reference Rs527236210(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 ClinVar
CLNACC RCV000133457.1,