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rs1060502471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502471(-;-)
Make rs1060502471(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32371075
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502471
dbSNP (old)rs1060502471
ClinGenrs1060502471
ebirs1060502471
HLIrs1060502471
Exacrs1060502471
Gnomadrs1060502471
Varsomers1060502471
LitVarrs1060502471
Maprs1060502471
PheGenIrs1060502471
Biobankrs1060502471
1000 genomesrs1060502471
hgdprs1060502471
ensemblrs1060502471
gopubmedrs1060502471
geneviewrs1060502471
scholarrs1060502471
googlers1060502471
pharmgkbrs1060502471
gwascentralrs1060502471
openSNPrs1060502471
23andMers1060502471
23andMe allrs1060502471
SNPshotrs1060502471
SNPdbers1060502471
MSV3drs1060502471
GWAS Ctlgrs1060502471
Max Magnitude0
ClinVar
Risk rs1060502471(-;-)
Alt rs1060502471(-;-)
Reference Rs1060502471(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.32945212delT
CLNSRC
CLNACC RCV000470808.1,