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rs1060502414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502414(C;T)
Make rs1060502414(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336945
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502414
dbSNP (old)rs1060502414
ClinGenrs1060502414
ebirs1060502414
HLIrs1060502414
Exacrs1060502414
Gnomadrs1060502414
Varsomers1060502414
Maprs1060502414
PheGenIrs1060502414
Biobankrs1060502414
1000 genomesrs1060502414
hgdprs1060502414
ensemblrs1060502414
gopubmedrs1060502414
geneviewrs1060502414
scholarrs1060502414
googlers1060502414
pharmgkbrs1060502414
gwascentralrs1060502414
openSNPrs1060502414
23andMers1060502414
23andMe allrs1060502414
SNPshotrs1060502414
SNPdbers1060502414
MSV3drs1060502414
GWAS Ctlgrs1060502414
Max Magnitude0
ClinVar
Risk rs1060502414(T;T)
Alt rs1060502414(T;T)
Reference Rs1060502414(C;C)
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.32911082C>T
CLNSRC
CLNACC RCV000461340.1,