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rs786203811

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs786203811(-;-)
Make rs786203811(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214728861
GeneBARD1
is asnp
is mentioned by
dbSNPrs786203811
ebirs786203811
HLIrs786203811
Exacrs786203811
Varsomers786203811
Maprs786203811
PheGenIrs786203811
hapmaprs786203811
1000 genomesrs786203811
hgdprs786203811
ensemblrs786203811
gopubmedrs786203811
geneviewrs786203811
scholarrs786203811
googlers786203811
pharmgkbrs786203811
gwascentralrs786203811
openSNPrs786203811
23andMers786203811
23andMe allrs786203811
SNP Nexus

SNPshotrs786203811
SNPdbers786203811
MSV3drs786203811
GWAS Ctlgrs786203811
Max Magnitude0
ClinVar
Risk rs786203811(;)
Alt rs786203811(;)
Reference rs786203811(CA;CA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215593585_215593586delTG
CLNSRC
CLNACC RCV000167280.1,