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rs1060501310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501310(C;C)
Make rs1060501310(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position214752446
GeneBARD1
is asnp
is mentioned by
dbSNPrs1060501310
dbSNP (old)rs1060501310
ClinGenrs1060501310
ebirs1060501310
HLIrs1060501310
Exacrs1060501310
Gnomadrs1060501310
Varsomers1060501310
Maprs1060501310
PheGenIrs1060501310
Biobankrs1060501310
1000 genomesrs1060501310
hgdprs1060501310
ensemblrs1060501310
gopubmedrs1060501310
geneviewrs1060501310
scholarrs1060501310
googlers1060501310
pharmgkbrs1060501310
gwascentralrs1060501310
openSNPrs1060501310
23andMers1060501310
23andMe allrs1060501310
SNPshotrs1060501310
SNPdbers1060501310
MSV3drs1060501310
GWAS Ctlgrs1060501310
Max Magnitude0
ClinVar
Risk rs1060501310(C;C)
Alt rs1060501310(C;C)
Reference Rs1060501310(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BARD1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000002.11:g.215617170C>G
CLNSRC
CLNACC RCV000474756.1,