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rs587780035

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780035(C;G)
Make rs587780035(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214781165
GeneBARD1
is asnp
is mentioned by
dbSNPrs587780035
ebirs587780035
HLIrs587780035
Exacrs587780035
Varsomers587780035
Maprs587780035
PheGenIrs587780035
hapmaprs587780035
1000 genomesrs587780035
hgdprs587780035
ensemblrs587780035
gopubmedrs587780035
geneviewrs587780035
scholarrs587780035
googlers587780035
pharmgkbrs587780035
gwascentralrs587780035
openSNPrs587780035
23andMers587780035
23andMe allrs587780035
SNP Nexus

SNPshotrs587780035
SNPdbers587780035
MSV3drs587780035
GWAS Ctlgrs587780035
Max Magnitude0
ClinVar
Risk rs587780035(G,T;G,T)
Alt rs587780035(G,T;G,T)
Reference rs587780035(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Variation info
Gene BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Reversed 1
HGVS NC_000002.11:g.215645889G>A; NC_000002.11:g.215645889G>C
CLNSRC
CLNACC RCV000221541.1, RCV000115641.5, RCV000205761.1, RCV000212120.1,