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rs587781974

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781974(-;-)
Make rs587781974(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61686146
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781974
ebirs587781974
HLIrs587781974
Exacrs587781974
Varsomers587781974
Maprs587781974
PheGenIrs587781974
hapmaprs587781974
1000 genomesrs587781974
hgdprs587781974
ensemblrs587781974
gopubmedrs587781974
geneviewrs587781974
scholarrs587781974
googlers587781974
pharmgkbrs587781974
gwascentralrs587781974
openSNPrs587781974
23andMers587781974
23andMe allrs587781974
SNP Nexus

SNPshotrs587781974
SNPdbers587781974
MSV3drs587781974
GWAS Ctlgrs587781974
Max Magnitude0
ClinVar
Risk rs587781974(;)
Alt rs587781974(;)
Reference rs587781974(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59763507delC
CLNSRC
CLNACC RCV000130366.2,