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rs1060499566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499566(A;A)
Make rs1060499566(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32316421
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060499566
dbSNP (old)rs1060499566
ClinGenrs1060499566
ebirs1060499566
HLIrs1060499566
Exacrs1060499566
Gnomadrs1060499566
Varsomers1060499566
LitVarrs1060499566
Maprs1060499566
PheGenIrs1060499566
Biobankrs1060499566
1000 genomesrs1060499566
hgdprs1060499566
ensemblrs1060499566
gopubmedrs1060499566
geneviewrs1060499566
scholarrs1060499566
googlers1060499566
pharmgkbrs1060499566
gwascentralrs1060499566
openSNPrs1060499566
23andMers1060499566
23andMe allrs1060499566
SNPshotrs1060499566
SNPdbers1060499566
MSV3drs1060499566
GWAS Ctlgrs1060499566
Max Magnitude0
ClinVar
Risk rs1060499566(A;A)
Alt rs1060499566(A;A)
Reference Rs1060499566(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32890558G>A
CLNSRC
CLNACC RCV000456118.1,