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rs587782173

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782173(A;A)
Make rs587782173(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43104867
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587782173
ebirs587782173
HLIrs587782173
Exacrs587782173
Varsomers587782173
Maprs587782173
PheGenIrs587782173
hapmaprs587782173
1000 genomesrs587782173
hgdprs587782173
ensemblrs587782173
gopubmedrs587782173
geneviewrs587782173
scholarrs587782173
googlers587782173
pharmgkbrs587782173
gwascentralrs587782173
openSNPrs587782173
23andMers587782173
23andMe allrs587782173
SNP Nexus

SNPshotrs587782173
SNPdbers587782173
MSV3drs587782173
GWAS Ctlgrs587782173
Max Magnitude0
ClinVar
Risk rs587782173(A,C,T;A,C,T)
Alt rs587782173(A,C,T;A,C,T)
Reference rs587782173(G;G)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41256884C>A; NC_000017.10:g.41256884C>T
CLNSRC
CLNACC RCV000236488.1, RCV000130778.2,