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rs587782410

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782410(G;G)
Make rs587782410(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61685976
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587782410
ebirs587782410
HLIrs587782410
Exacrs587782410
Varsomers587782410
Maprs587782410
PheGenIrs587782410
hapmaprs587782410
1000 genomesrs587782410
hgdprs587782410
ensemblrs587782410
gopubmedrs587782410
geneviewrs587782410
scholarrs587782410
googlers587782410
pharmgkbrs587782410
gwascentralrs587782410
openSNPrs587782410
23andMers587782410
23andMe allrs587782410
SNP Nexus

SNPshotrs587782410
SNPdbers587782410
MSV3drs587782410
GWAS Ctlgrs587782410
Max Magnitude0
ClinVar
Risk rs587782410(G;G)
Alt rs587782410(G;G)
Reference rs587782410(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.59763337A>C
CLNSRC
CLNACC RCV000131449.2, RCV000216847.1,