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rs1060502385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTA;GTA) 0 common in clinvar
Make rs1060502385(GTA;TT)
Make rs1060502385(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32332376
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502385
dbSNP (old)rs1060502385
ClinGenrs1060502385
ebirs1060502385
HLIrs1060502385
Exacrs1060502385
Gnomadrs1060502385
Varsomers1060502385
Maprs1060502385
PheGenIrs1060502385
Biobankrs1060502385
1000 genomesrs1060502385
hgdprs1060502385
ensemblrs1060502385
gopubmedrs1060502385
geneviewrs1060502385
scholarrs1060502385
googlers1060502385
pharmgkbrs1060502385
gwascentralrs1060502385
openSNPrs1060502385
23andMers1060502385
23andMe allrs1060502385
SNPshotrs1060502385
SNPdbers1060502385
MSV3drs1060502385
GWAS Ctlgrs1060502385
Max Magnitude0
ClinVar
Risk rs1060502385(TT;TT)
Alt rs1060502385(TT;TT)
Reference Rs1060502385(GTA;GTA)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32906513_32906515delGTAinsTT
CLNSRC
CLNACC RCV000470864.1,