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rs1060502484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502484(-;-)
Make rs1060502484(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336590
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502484
dbSNP (old)rs1060502484
ClinGenrs1060502484
ebirs1060502484
HLIrs1060502484
Exacrs1060502484
Gnomadrs1060502484
Varsomers1060502484
Maprs1060502484
PheGenIrs1060502484
Biobankrs1060502484
1000 genomesrs1060502484
hgdprs1060502484
ensemblrs1060502484
gopubmedrs1060502484
geneviewrs1060502484
scholarrs1060502484
googlers1060502484
pharmgkbrs1060502484
gwascentralrs1060502484
openSNPrs1060502484
23andMers1060502484
23andMe allrs1060502484
SNPshotrs1060502484
SNPdbers1060502484
MSV3drs1060502484
GWAS Ctlgrs1060502484
Max Magnitude0
ClinVar
Risk rs1060502484(-;-)
Alt rs1060502484(-;-)
Reference Rs1060502484(A;A)
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.32910727delA
CLNSRC
CLNACC RCV000469931.1,