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rs1060502360

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502360(-;-)
Make rs1060502360(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43094787
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502360
dbSNP (classic)rs1060502360
ClinGenrs1060502360
ebirs1060502360
HLIrs1060502360
Exacrs1060502360
Gnomadrs1060502360
Varsomers1060502360
LitVarrs1060502360
Maprs1060502360
PheGenIrs1060502360
Biobankrs1060502360
1000 genomesrs1060502360
hgdprs1060502360
ensemblrs1060502360
geneviewrs1060502360
scholarrs1060502360
googlers1060502360
pharmgkbrs1060502360
gwascentralrs1060502360
openSNPrs1060502360
23andMers1060502360
23andMe allrs1060502360
SNPshotrs1060502360
SNPdbers1060502360
MSV3drs1060502360
GWAS Ctlgrs1060502360
Max Magnitude0
ClinVar
Risk rs1060502360(-;-)
Alt rs1060502360(-;-)
Reference Rs1060502360(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41246804delG
CLNSRC
CLNACC RCV000458382.1,