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rs786203533

From SNPedia

Orientationminus
Geno Mag Summary
(GTGA;GTGA) 0 common in clinvar
Make rs786203533(ATG;ATG)
Make rs786203533(ATG;GTGA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214780607
GeneBARD1
is asnp
is mentioned by
dbSNPrs786203533
ebirs786203533
HLIrs786203533
Exacrs786203533
Varsomers786203533
Maprs786203533
PheGenIrs786203533
hapmaprs786203533
1000 genomesrs786203533
hgdprs786203533
ensemblrs786203533
gopubmedrs786203533
geneviewrs786203533
scholarrs786203533
googlers786203533
pharmgkbrs786203533
gwascentralrs786203533
openSNPrs786203533
23andMers786203533
23andMe allrs786203533
SNP Nexus

SNPshotrs786203533
SNPdbers786203533
MSV3drs786203533
GWAS Ctlgrs786203533
Max Magnitude0
ClinVar
Risk rs786203533(ATG;ATG)
Alt rs786203533(ATG;ATG)
Reference rs786203533(GTGA;GTGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645331_215645334delTCACinsCAT
CLNSRC
CLNACC RCV000166882.1,