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rs1060505047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060505047(-;-)
Make rs1060505047(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43091696
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060505047
dbSNP (old)rs1060505047
ClinGenrs1060505047
ebirs1060505047
HLIrs1060505047
Exacrs1060505047
Gnomadrs1060505047
Varsomers1060505047
Maprs1060505047
PheGenIrs1060505047
Biobankrs1060505047
1000 genomesrs1060505047
hgdprs1060505047
ensemblrs1060505047
gopubmedrs1060505047
geneviewrs1060505047
scholarrs1060505047
googlers1060505047
pharmgkbrs1060505047
gwascentralrs1060505047
openSNPrs1060505047
23andMers1060505047
23andMe allrs1060505047
SNPshotrs1060505047
SNPdbers1060505047
MSV3drs1060505047
GWAS Ctlgrs1060505047
Max Magnitude0
ClinVar
Risk rs1060505047(-;-)
Alt rs1060505047(-;-)
Reference Rs1060505047(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.41243713delC
CLNSRC
CLNACC RCV000477804.1,