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rs1060502454

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502454(-;-)
Make rs1060502454(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32332437
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502454
dbSNP (classic)rs1060502454
ClinGenrs1060502454
ebirs1060502454
HLIrs1060502454
Exacrs1060502454
Gnomadrs1060502454
Varsomers1060502454
LitVarrs1060502454
Maprs1060502454
PheGenIrs1060502454
Biobankrs1060502454
1000 genomesrs1060502454
hgdprs1060502454
ensemblrs1060502454
geneviewrs1060502454
scholarrs1060502454
googlers1060502454
pharmgkbrs1060502454
gwascentralrs1060502454
openSNPrs1060502454
23andMers1060502454
23andMe allrs1060502454
SNPshotrs1060502454
SNPdbers1060502454
MSV3drs1060502454
GWAS Ctlgrs1060502454
Max Magnitude0
ClinVar
Risk rs1060502454(-;-)
Alt rs1060502454(-;-)
Reference Rs1060502454(T;T)
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.32906574delT
CLNSRC
CLNACC RCV000470359.1,