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rs587781786

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781786(C;T)
Make rs587781786(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61849173
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781786
ebirs587781786
HLIrs587781786
Exacrs587781786
Varsomers587781786
Maprs587781786
PheGenIrs587781786
hapmaprs587781786
1000 genomesrs587781786
hgdprs587781786
ensemblrs587781786
gopubmedrs587781786
geneviewrs587781786
scholarrs587781786
googlers587781786
pharmgkbrs587781786
gwascentralrs587781786
openSNPrs587781786
23andMers587781786
23andMe allrs587781786
SNP Nexus

SNPshotrs587781786
SNPdbers587781786
MSV3drs587781786
GWAS Ctlgrs587781786
Max Magnitude0
ClinVar
Risk rs587781786(T;T)
Alt rs587781786(T;T)
Reference rs587781786(C;C)
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.59926534G>A
CLNSRC
CLNACC RCV000130041.2, RCV000213568.1,