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rs1060502376

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502376(G;T)
Make rs1060502376(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32319076
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502376
dbSNP (old)rs1060502376
ClinGenrs1060502376
ebirs1060502376
HLIrs1060502376
Exacrs1060502376
Gnomadrs1060502376
Varsomers1060502376
Maprs1060502376
PheGenIrs1060502376
Biobankrs1060502376
1000 genomesrs1060502376
hgdprs1060502376
ensemblrs1060502376
gopubmedrs1060502376
geneviewrs1060502376
scholarrs1060502376
googlers1060502376
pharmgkbrs1060502376
gwascentralrs1060502376
openSNPrs1060502376
23andMers1060502376
23andMe allrs1060502376
SNPshotrs1060502376
SNPdbers1060502376
MSV3drs1060502376
GWAS Ctlgrs1060502376
Max Magnitude0
ClinVar
Risk rs1060502376(T;T)
Alt rs1060502376(T;T)
Reference Rs1060502376(G;G)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome not specified
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32893213G>T
CLNSRC
CLNACC RCV000458301.1, RCV000483572.1,