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

rs1060502345

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(ATC;ATC) 0 common in clinvar
Make rs1060502345(ATC;T)
Make rs1060502345(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43091465
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1060502345
dbSNP (old)rs1060502345
ClinGenrs1060502345
ebirs1060502345
HLIrs1060502345
Exacrs1060502345
Gnomadrs1060502345
Varsomers1060502345
Maprs1060502345
PheGenIrs1060502345
Biobankrs1060502345
1000 genomesrs1060502345
hgdprs1060502345
ensemblrs1060502345
gopubmedrs1060502345
geneviewrs1060502345
scholarrs1060502345
googlers1060502345
pharmgkbrs1060502345
gwascentralrs1060502345
openSNPrs1060502345
23andMers1060502345
23andMe allrs1060502345
SNPshotrs1060502345
SNPdbers1060502345
MSV3drs1060502345
GWAS Ctlgrs1060502345
Max Magnitude0
ClinVar
Risk rs1060502345(T;T)
Alt rs1060502345(T;T)
Reference Rs1060502345(ATC;ATC)
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.41243482_41243484delGATinsA
CLNSRC
CLNACC RCV000458817.1,