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rs587780033

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780033(-;-)
Make rs587780033(-;A)
Make rs587780033(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781250
GeneBARD1
is asnp
is mentioned by
dbSNPrs587780033
ebirs587780033
HLIrs587780033
Exacrs587780033
Varsomers587780033
Maprs587780033
PheGenIrs587780033
hapmaprs587780033
1000 genomesrs587780033
hgdprs587780033
ensemblrs587780033
gopubmedrs587780033
geneviewrs587780033
scholarrs587780033
googlers587780033
pharmgkbrs587780033
gwascentralrs587780033
openSNPrs587780033
23andMers587780033
23andMe allrs587780033
SNP Nexus

SNPshotrs587780033
SNPdbers587780033
MSV3drs587780033
GWAS Ctlgrs587780033
Max Magnitude0
ClinVar
Risk rs587780033(A;A)
Alt rs587780033(A;A)
Reference rs587780033(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645975dupT
CLNSRC
CLNACC RCV000115638.3,