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rs1060502430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502430(-;-)
Make rs1060502430(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32340008
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502430
dbSNP (old)rs1060502430
ClinGenrs1060502430
ebirs1060502430
HLIrs1060502430
Exacrs1060502430
Gnomadrs1060502430
Varsomers1060502430
Maprs1060502430
PheGenIrs1060502430
Biobankrs1060502430
1000 genomesrs1060502430
hgdprs1060502430
ensemblrs1060502430
gopubmedrs1060502430
geneviewrs1060502430
scholarrs1060502430
googlers1060502430
pharmgkbrs1060502430
gwascentralrs1060502430
openSNPrs1060502430
23andMers1060502430
23andMe allrs1060502430
SNPshotrs1060502430
SNPdbers1060502430
MSV3drs1060502430
GWAS Ctlgrs1060502430
Max Magnitude0
ClinVar
Risk rs1060502430(-;-)
Alt rs1060502430(-;-)
Reference Rs1060502430(T;T)
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.32914145delT
CLNSRC
CLNACC RCV000476395.1,