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rs786203891

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203891(-;-)
Make rs786203891(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214780676
GeneBARD1
is asnp
is mentioned by
dbSNPrs786203891
ebirs786203891
HLIrs786203891
Exacrs786203891
Varsomers786203891
Maprs786203891
PheGenIrs786203891
hapmaprs786203891
1000 genomesrs786203891
hgdprs786203891
ensemblrs786203891
gopubmedrs786203891
geneviewrs786203891
scholarrs786203891
googlers786203891
pharmgkbrs786203891
gwascentralrs786203891
openSNPrs786203891
23andMers786203891
23andMe allrs786203891
SNP Nexus

SNPshotrs786203891
SNPdbers786203891
MSV3drs786203891
GWAS Ctlgrs786203891
Max Magnitude0
ClinVar
Risk rs786203891(;)
Alt rs786203891(;)
Reference rs786203891(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645400delT
CLNSRC
CLNACC RCV000167393.1,