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rs779427628

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs779427628(-;-)
Make rs779427628(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781334
GeneBARD1
is asnp
is mentioned by
dbSNPrs779427628
ebirs779427628
HLIrs779427628
Exacrs779427628
Varsomers779427628
Maprs779427628
PheGenIrs779427628
hapmaprs779427628
1000 genomesrs779427628
hgdprs779427628
ensemblrs779427628
gopubmedrs779427628
geneviewrs779427628
scholarrs779427628
googlers779427628
pharmgkbrs779427628
gwascentralrs779427628
openSNPrs779427628
23andMers779427628
23andMe allrs779427628
SNP Nexus

SNPshotrs779427628
SNPdbers779427628
MSV3drs779427628
GWAS Ctlgrs779427628
Max Magnitude0
ClinVar
Risk rs779427628(;)
Alt rs779427628(;)
Reference rs779427628(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.215646058_215646059delAT
CLNSRC
CLNACC RCV000166193.1,