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rs1060502332

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502332(AA;AA)
Make rs1060502332(AA;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43093401
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502332
dbSNP (old)rs1060502332
ClinGenrs1060502332
ebirs1060502332
HLIrs1060502332
Exacrs1060502332
Gnomadrs1060502332
Varsomers1060502332
Maprs1060502332
PheGenIrs1060502332
Biobankrs1060502332
1000 genomesrs1060502332
hgdprs1060502332
ensemblrs1060502332
gopubmedrs1060502332
geneviewrs1060502332
scholarrs1060502332
googlers1060502332
pharmgkbrs1060502332
gwascentralrs1060502332
openSNPrs1060502332
23andMers1060502332
23andMe allrs1060502332
SNPshotrs1060502332
SNPdbers1060502332
MSV3drs1060502332
GWAS Ctlgrs1060502332
Max Magnitude0
ClinVar
Risk rs1060502332(AA;AA)
Alt rs1060502332(AA;AA)
Reference Rs1060502332(T;T)
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.41245418delAinsTT
CLNSRC
CLNACC RCV000475379.1,