Have questions? Visit https://www.reddit.com/r/SNPedia

rs527236197

From SNPedia

Merged intors193303002
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236197(A;A)
Make rs527236197(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15927
is asnp
is mentioned by
dbSNPrs527236197
ebirs527236197
HLIrs527236197
Exacrs527236197
Varsomers527236197
Maprs527236197
PheGenIrs527236197
hapmaprs527236197
1000 genomesrs527236197
hgdprs527236197
ensemblrs527236197
gopubmedrs527236197
geneviewrs527236197
scholarrs527236197
googlers527236197
pharmgkbrs527236197
gwascentralrs527236197
openSNPrs527236197
23andMers527236197
23andMe allrs527236197
SNP Nexus

SNPshotrs527236197
SNPdbers527236197
MSV3drs527236197
GWAS Ctlgrs527236197
StatusMerged into rs193303002
Max Magnitude0
ClinVar
Risk rs527236197(A;A)
Alt rs527236197(A;A)
Reference rs527236197(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15927G>A
CLNSRC
CLNACC RCV000133441.1,