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rs1060502433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502433(A;A)
Make rs1060502433(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32357846
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502433
dbSNP (old)rs1060502433
ClinGenrs1060502433
ebirs1060502433
HLIrs1060502433
Exacrs1060502433
Gnomadrs1060502433
Varsomers1060502433
LitVarrs1060502433
Maprs1060502433
PheGenIrs1060502433
Biobankrs1060502433
1000 genomesrs1060502433
hgdprs1060502433
ensemblrs1060502433
gopubmedrs1060502433
geneviewrs1060502433
scholarrs1060502433
googlers1060502433
pharmgkbrs1060502433
gwascentralrs1060502433
openSNPrs1060502433
23andMers1060502433
23andMe allrs1060502433
SNPshotrs1060502433
SNPdbers1060502433
MSV3drs1060502433
GWAS Ctlgrs1060502433
Max Magnitude0
ClinVar
Risk rs1060502433(A;A)
Alt rs1060502433(A;A)
Reference Rs1060502433(G;G)
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.32931983G>A
CLNSRC
CLNACC RCV000472083.1,