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rs1060501287

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501287(-;-)
Make rs1060501287(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position214769302
GeneBARD1
is asnp
is mentioned by
dbSNPrs1060501287
dbSNP (old)rs1060501287
ClinGenrs1060501287
ebirs1060501287
HLIrs1060501287
Exacrs1060501287
Gnomadrs1060501287
Varsomers1060501287
Maprs1060501287
PheGenIrs1060501287
Biobankrs1060501287
1000 genomesrs1060501287
hgdprs1060501287
ensemblrs1060501287
gopubmedrs1060501287
geneviewrs1060501287
scholarrs1060501287
googlers1060501287
pharmgkbrs1060501287
gwascentralrs1060501287
openSNPrs1060501287
23andMers1060501287
23andMe allrs1060501287
SNPshotrs1060501287
SNPdbers1060501287
MSV3drs1060501287
GWAS Ctlgrs1060501287
Max Magnitude0
ClinVar
Risk rs1060501287(-;-)
Alt rs1060501287(-;-)
Reference Rs1060501287(C;C)
Significance Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene BARD1
CLNDBN Familial cancer of breast not provided
Reversed 1
HGVS NC_000002.11:g.215634026delG
CLNSRC
CLNACC RCV000461547.1, RCV000483503.1,