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rs1060502485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502485(A;A)
Make rs1060502485(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32326100
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502485
dbSNP (old)rs1060502485
ClinGenrs1060502485
ebirs1060502485
HLIrs1060502485
Exacrs1060502485
Gnomadrs1060502485
Varsomers1060502485
LitVarrs1060502485
Maprs1060502485
PheGenIrs1060502485
Biobankrs1060502485
1000 genomesrs1060502485
hgdprs1060502485
ensemblrs1060502485
gopubmedrs1060502485
geneviewrs1060502485
scholarrs1060502485
googlers1060502485
pharmgkbrs1060502485
gwascentralrs1060502485
openSNPrs1060502485
23andMers1060502485
23andMe allrs1060502485
SNPshotrs1060502485
SNPdbers1060502485
MSV3drs1060502485
GWAS Ctlgrs1060502485
Max Magnitude0
ClinVar
Risk rs1060502485(A;A)
Alt rs1060502485(A;A)
Reference Rs1060502485(G;G)
Significance Probable-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.32900237G>A
CLNSRC
CLNACC RCV000470985.1,