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rs527236172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236172(A;G)
Make rs527236172(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15098
GeneCYTB
is asnp
is mentioned by
dbSNPrs527236172
dbSNP (old)rs527236172
ClinGenrs527236172
ebirs527236172
HLIrs527236172
Exacrs527236172
Gnomadrs527236172
Varsomers527236172
Maprs527236172
PheGenIrs527236172
Biobankrs527236172
1000 genomesrs527236172
hgdprs527236172
ensemblrs527236172
gopubmedrs527236172
geneviewrs527236172
scholarrs527236172
googlers527236172
pharmgkbrs527236172
gwascentralrs527236172
openSNPrs527236172
23andMers527236172
23andMe allrs527236172
SNP Nexus

SNPshotrs527236172
SNPdbers527236172
MSV3drs527236172
GWAS Ctlgrs527236172
Max Magnitude0
ClinVar
Risk rs527236172(G;G)
Alt rs527236172(G;G)
Reference Rs527236172(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of ovary
Variation info
Gene CYTB
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_012920.1:m.15098A>G
CLNSRC ClinVar
CLNACC RCV000133414.1,