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rs1060499833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499833(G;G)
Make rs1060499833(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32339338
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060499833
dbSNP (old)rs1060499833
ClinGenrs1060499833
ebirs1060499833
HLIrs1060499833
Exacrs1060499833
Gnomadrs1060499833
Varsomers1060499833
Maprs1060499833
PheGenIrs1060499833
Biobankrs1060499833
1000 genomesrs1060499833
hgdprs1060499833
ensemblrs1060499833
gopubmedrs1060499833
geneviewrs1060499833
scholarrs1060499833
googlers1060499833
pharmgkbrs1060499833
gwascentralrs1060499833
openSNPrs1060499833
23andMers1060499833
23andMe allrs1060499833
SNPshotrs1060499833
SNPdbers1060499833
MSV3drs1060499833
GWAS Ctlgrs1060499833
Max Magnitude0
ClinVar
Risk rs1060499833(G;G)
Alt rs1060499833(G;G)
Reference Rs1060499833(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913475T>G
CLNSRC
CLNACC RCV000469488.1,