Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203739

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203739(-;-)
Make rs786203739(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214730442
GeneBARD1
is asnp
is mentioned by
dbSNPrs786203739
ebirs786203739
HLIrs786203739
Exacrs786203739
Varsomers786203739
Maprs786203739
PheGenIrs786203739
hapmaprs786203739
1000 genomesrs786203739
hgdprs786203739
ensemblrs786203739
gopubmedrs786203739
geneviewrs786203739
scholarrs786203739
googlers786203739
pharmgkbrs786203739
gwascentralrs786203739
openSNPrs786203739
23andMers786203739
23andMe allrs786203739
SNP Nexus

SNPshotrs786203739
SNPdbers786203739
MSV3drs786203739
GWAS Ctlgrs786203739
Max Magnitude0
ClinVar
Risk rs786203739(;)
Alt rs786203739(;)
Reference rs786203739(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.215595166delG
CLNSRC
CLNACC RCV000167174.1,