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rs200265692

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs200265692(A;G)
Make rs200265692(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339435
GeneBRCA2
is asnp
is mentioned by
dbSNPrs200265692
ebirs200265692
HLIrs200265692
Exacrs200265692
Varsomers200265692
Maprs200265692
PheGenIrs200265692
hapmaprs200265692
1000 genomesrs200265692
hgdprs200265692
ensemblrs200265692
gopubmedrs200265692
geneviewrs200265692
scholarrs200265692
googlers200265692
pharmgkbrs200265692
gwascentralrs200265692
openSNPrs200265692
23andMers200265692
23andMe allrs200265692
SNP Nexus

SNPshotrs200265692
SNPdbers200265692
MSV3drs200265692
GWAS Ctlgrs200265692
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs200265692(G,T;G,T)
Alt rs200265692(G,T;G,T)
Reference rs200265692(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913572A>G; NC_000013.10:g.32913572A>T
CLNSRC ClinVar
CLNACC RCV000165787.1, RCV000031525.3,