Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502334(A;A)
Make rs1060502334(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43093258
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502334
dbSNP (old)rs1060502334
ClinGenrs1060502334
ebirs1060502334
HLIrs1060502334
Exacrs1060502334
Gnomadrs1060502334
Varsomers1060502334
Maprs1060502334
PheGenIrs1060502334
Biobankrs1060502334
1000 genomesrs1060502334
hgdprs1060502334
ensemblrs1060502334
gopubmedrs1060502334
geneviewrs1060502334
scholarrs1060502334
googlers1060502334
pharmgkbrs1060502334
gwascentralrs1060502334
openSNPrs1060502334
23andMers1060502334
23andMe allrs1060502334
SNPshotrs1060502334
SNPdbers1060502334
MSV3drs1060502334
GWAS Ctlgrs1060502334
Max Magnitude0
ClinVar
Risk rs1060502334(A;A)
Alt rs1060502334(A;A)
Reference Rs1060502334(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.41245275A>T
CLNSRC
CLNACC RCV000475494.1,