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

rs587776485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587776485(-;-)
Make rs587776485(-;CA)
ReferenceGRCh38 38.1/142
Chromosome17
Position43104895
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587776485
ebirs587776485
HLIrs587776485
Exacrs587776485
Varsomers587776485
Maprs587776485
PheGenIrs587776485
hapmaprs587776485
1000 genomesrs587776485
hgdprs587776485
ensemblrs587776485
gopubmedrs587776485
geneviewrs587776485
scholarrs587776485
googlers587776485
pharmgkbrs587776485
gwascentralrs587776485
openSNPrs587776485
23andMers587776485
23andMe allrs587776485
SNP Nexus

SNPshotrs587776485
SNPdbers587776485
MSV3drs587776485
GWAS Ctlgrs587776485
Max Magnitude0
ClinVar
Risk rs587776485(;)
Alt rs587776485(;)
Reference rs587776485(CA;CA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000017.10:g.41256912_41256913delCA
CLNSRC ClinVar
CLNACC RCV000144206.1,