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rs587781487

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781487(-;-)
Make rs587781487(-;T)
Make rs587781487(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43099809
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587781487
ebirs587781487
HLIrs587781487
Exacrs587781487
Varsomers587781487
Maprs587781487
PheGenIrs587781487
hapmaprs587781487
1000 genomesrs587781487
hgdprs587781487
ensemblrs587781487
gopubmedrs587781487
geneviewrs587781487
scholarrs587781487
googlers587781487
pharmgkbrs587781487
gwascentralrs587781487
openSNPrs587781487
23andMers587781487
23andMe allrs587781487
SNP Nexus

SNPshotrs587781487
SNPdbers587781487
MSV3drs587781487
GWAS Ctlgrs587781487
Max Magnitude0
ClinVar
Risk rs587781487(T;T)
Alt rs587781487(T;T)
Reference rs587781487(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41251827dupA
CLNSRC
CLNACC RCV000129450.2, RCV000168444.1, RCV000236963.1,