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rs786201868

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786201868(-;-)
Make rs786201868(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214781013
GeneBARD1
is asnp
is mentioned by
dbSNPrs786201868
ebirs786201868
HLIrs786201868
Exacrs786201868
Varsomers786201868
Maprs786201868
PheGenIrs786201868
hapmaprs786201868
1000 genomesrs786201868
hgdprs786201868
ensemblrs786201868
gopubmedrs786201868
geneviewrs786201868
scholarrs786201868
googlers786201868
pharmgkbrs786201868
gwascentralrs786201868
openSNPrs786201868
23andMers786201868
23andMe allrs786201868
SNP Nexus

SNPshotrs786201868
SNPdbers786201868
MSV3drs786201868
GWAS Ctlgrs786201868
Max Magnitude0
ClinVar
Risk rs786201868(;)
Alt rs786201868(;)
Reference rs786201868(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645737_215645738delCT
CLNSRC
CLNACC RCV000164367.1,