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rs587780875

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780875(C;C)
Make rs587780875(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61793687
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587780875
ebirs587780875
HLIrs587780875
Exacrs587780875
Varsomers587780875
Maprs587780875
PheGenIrs587780875
hapmaprs587780875
1000 genomesrs587780875
hgdprs587780875
ensemblrs587780875
gopubmedrs587780875
geneviewrs587780875
scholarrs587780875
googlers587780875
pharmgkbrs587780875
gwascentralrs587780875
openSNPrs587780875
23andMers587780875
23andMe allrs587780875
SNP Nexus

SNPshotrs587780875
SNPdbers587780875
MSV3drs587780875
GWAS Ctlgrs587780875
Max Magnitude0
ClinVar
Risk rs587780875(C,G;C,G)
Alt rs587780875(C,G;C,G)
Reference rs587780875(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.59871048A>C; NC_000017.10:g.59871048A>G
CLNSRC
CLNACC RCV000195948.1, RCV000124034.5, RCV000205219.1, RCV000212310.1,