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rs866676518

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs866676518(-;-)
Make rs866676518(-;C)
Make rs866676518(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339045
GeneBRCA2
is asnp
is mentioned by
dbSNPrs866676518
ebirs866676518
HLIrs866676518
Exacrs866676518
Varsomers866676518
Maprs866676518
PheGenIrs866676518
hapmaprs866676518
1000 genomesrs866676518
hgdprs866676518
ensemblrs866676518
gopubmedrs866676518
geneviewrs866676518
scholarrs866676518
googlers866676518
pharmgkbrs866676518
gwascentralrs866676518
openSNPrs866676518
23andMers866676518
23andMe allrs866676518
SNP Nexus

SNPshotrs866676518
SNPdbers866676518
MSV3drs866676518
GWAS Ctlgrs866676518
Max Magnitude0
ClinVar
Risk rs866676518(C;C)
Alt rs866676518(C;C)
Reference rs866676518(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913183dupC
CLNSRC
CLNACC RCV000168306.2,