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rs786202559

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202559(C;G)
Make rs786202559(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214780813
GeneBARD1
is asnp
is mentioned by
dbSNPrs786202559
ebirs786202559
HLIrs786202559
Exacrs786202559
Varsomers786202559
Maprs786202559
PheGenIrs786202559
hapmaprs786202559
1000 genomesrs786202559
hgdprs786202559
ensemblrs786202559
gopubmedrs786202559
geneviewrs786202559
scholarrs786202559
googlers786202559
pharmgkbrs786202559
gwascentralrs786202559
openSNPrs786202559
23andMers786202559
23andMe allrs786202559
SNP Nexus

SNPshotrs786202559
SNPdbers786202559
MSV3drs786202559
GWAS Ctlgrs786202559
Max Magnitude0
ClinVar
Risk rs786202559(G;G)
Alt rs786202559(G;G)
Reference rs786202559(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645537G>C
CLNSRC
CLNACC RCV000165421.1,