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rs1060502444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1060502444(-;-)
Make rs1060502444(-;TC)
Make rs1060502444(TC;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32340429
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502444
dbSNP (classic)rs1060502444
ClinGenrs1060502444
ebirs1060502444
HLIrs1060502444
Exacrs1060502444
Gnomadrs1060502444
Varsomers1060502444
LitVarrs1060502444
Maprs1060502444
PheGenIrs1060502444
Biobankrs1060502444
1000 genomesrs1060502444
hgdprs1060502444
ensemblrs1060502444
geneviewrs1060502444
scholarrs1060502444
googlers1060502444
pharmgkbrs1060502444
gwascentralrs1060502444
openSNPrs1060502444
23andMers1060502444
23andMe allrs1060502444
SNPshotrs1060502444
SNPdbers1060502444
MSV3drs1060502444
GWAS Ctlgrs1060502444
Max Magnitude0
ClinVar
Risk rs1060502444(-;-)
Alt rs1060502444(-;-)
Reference Rs1060502444(CT;CT)
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.32914566_32914567delTC
CLNSRC
CLNACC RCV000463421.1,