Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780031

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780031(A;A)
Make rs587780031(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214809567
GeneBARD1, LOC101928103
is asnp
is mentioned by
dbSNPrs587780031
ebirs587780031
HLIrs587780031
Exacrs587780031
Varsomers587780031
Maprs587780031
PheGenIrs587780031
hapmaprs587780031
1000 genomesrs587780031
hgdprs587780031
ensemblrs587780031
gopubmedrs587780031
geneviewrs587780031
scholarrs587780031
googlers587780031
pharmgkbrs587780031
gwascentralrs587780031
openSNPrs587780031
23andMers587780031
23andMe allrs587780031
SNP Nexus

SNPshotrs587780031
SNPdbers587780031
MSV3drs587780031
GWAS Ctlgrs587780031
Max Magnitude0
ClinVar
Risk rs587780031(A;A)
Alt rs587780031(A;A)
Reference rs587780031(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC101928103 BARD1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.215674291C>T
CLNSRC
CLNACC RCV000115635.3,