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rs786202118

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202118(A;A)
Make rs786202118(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214728742
GeneBARD1
is asnp
is mentioned by
dbSNPrs786202118
ebirs786202118
HLIrs786202118
Exacrs786202118
Varsomers786202118
Maprs786202118
PheGenIrs786202118
hapmaprs786202118
1000 genomesrs786202118
hgdprs786202118
ensemblrs786202118
gopubmedrs786202118
geneviewrs786202118
scholarrs786202118
googlers786202118
pharmgkbrs786202118
gwascentralrs786202118
openSNPrs786202118
23andMers786202118
23andMe allrs786202118
SNP Nexus

SNPshotrs786202118
SNPdbers786202118
MSV3drs786202118
GWAS Ctlgrs786202118
Max Magnitude0
ClinVar
Risk rs786202118(A;A)
Alt rs786202118(A;A)
Reference rs786202118(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215593466C>T
CLNSRC
CLNACC RCV000164774.1,