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rs587782666

From SNPedia

Orientationminus
Geno Mag Summary
(ATAA;ATAA) 0 common in clinvar
Make rs587782666(-;-)
Make rs587782666(-;ATAA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43104225
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587782666
ebirs587782666
HLIrs587782666
Exacrs587782666
Varsomers587782666
Maprs587782666
PheGenIrs587782666
hapmaprs587782666
1000 genomesrs587782666
hgdprs587782666
ensemblrs587782666
gopubmedrs587782666
geneviewrs587782666
scholarrs587782666
googlers587782666
pharmgkbrs587782666
gwascentralrs587782666
openSNPrs587782666
23andMers587782666
23andMe allrs587782666
SNP Nexus

SNPshotrs587782666
SNPdbers587782666
MSV3drs587782666
GWAS Ctlgrs587782666
Max Magnitude0
ClinVar
Risk rs587782666(;)
Alt rs587782666(;)
Reference rs587782666(ATAA;ATAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41256242_41256245delTTAT
CLNSRC
CLNACC RCV000132087.2,