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rs1060502478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502478(-;-)
Make rs1060502478(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32362536
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502478
dbSNP (classic)rs1060502478
ClinGenrs1060502478
ebirs1060502478
HLIrs1060502478
Exacrs1060502478
Gnomadrs1060502478
Varsomers1060502478
LitVarrs1060502478
Maprs1060502478
PheGenIrs1060502478
Biobankrs1060502478
1000 genomesrs1060502478
hgdprs1060502478
ensemblrs1060502478
geneviewrs1060502478
scholarrs1060502478
googlers1060502478
pharmgkbrs1060502478
gwascentralrs1060502478
openSNPrs1060502478
23andMers1060502478
23andMe allrs1060502478
SNPshotrs1060502478
SNPdbers1060502478
MSV3drs1060502478
GWAS Ctlgrs1060502478
Max Magnitude0
ClinVar
Risk rs1060502478(-;-)
Alt rs1060502478(-;-)
Reference Rs1060502478(A;A)
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.32936673delA
CLNSRC
CLNACC RCV000470903.1,