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rs1060505052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060505052(-;-)
Make rs1060505052(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43099812
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060505052
dbSNP (classic)rs1060505052
ClinGenrs1060505052
ebirs1060505052
HLIrs1060505052
Exacrs1060505052
Gnomadrs1060505052
Varsomers1060505052
LitVarrs1060505052
Maprs1060505052
PheGenIrs1060505052
Biobankrs1060505052
1000 genomesrs1060505052
hgdprs1060505052
ensemblrs1060505052
geneviewrs1060505052
scholarrs1060505052
googlers1060505052
pharmgkbrs1060505052
gwascentralrs1060505052
openSNPrs1060505052
23andMers1060505052
SNPshotrs1060505052
SNPdbers1060505052
MSV3drs1060505052
GWAS Ctlgrs1060505052
Max Magnitude0
ClinVar
Risk rs1060505052(-;-)
Alt rs1060505052(-;-)
Reference Rs1060505052(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41251829delC
CLNSRC
CLNACC RCV000477866.1,