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rs1060502455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502455(-;-)
Make rs1060502455(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336337
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502455
dbSNP (classic)rs1060502455
ClinGenrs1060502455
ebirs1060502455
HLIrs1060502455
Exacrs1060502455
Gnomadrs1060502455
Varsomers1060502455
LitVarrs1060502455
Maprs1060502455
PheGenIrs1060502455
Biobankrs1060502455
1000 genomesrs1060502455
hgdprs1060502455
ensemblrs1060502455
geneviewrs1060502455
scholarrs1060502455
googlers1060502455
pharmgkbrs1060502455
gwascentralrs1060502455
openSNPrs1060502455
23andMers1060502455
23andMe allrs1060502455
SNPshotrs1060502455
SNPdbers1060502455
MSV3drs1060502455
GWAS Ctlgrs1060502455
Max Magnitude0
ClinVar
Risk rs1060502455(-;-)
Alt rs1060502455(-;-)
Reference Rs1060502455(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.32910474delG
CLNSRC
CLNACC RCV000458243.1,