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rs587780228

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780228(G;T)
Make rs587780228(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61793698
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587780228
ebirs587780228
HLIrs587780228
Exacrs587780228
Varsomers587780228
Maprs587780228
PheGenIrs587780228
hapmaprs587780228
1000 genomesrs587780228
hgdprs587780228
ensemblrs587780228
gopubmedrs587780228
geneviewrs587780228
scholarrs587780228
googlers587780228
pharmgkbrs587780228
gwascentralrs587780228
openSNPrs587780228
23andMers587780228
23andMe allrs587780228
SNP Nexus

SNPshotrs587780228
SNPdbers587780228
MSV3drs587780228
GWAS Ctlgrs587780228
Max Magnitude0
ClinVar
Risk rs587780228(T;T)
Alt rs587780228(T;T)
Reference rs587780228(G;G)
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.59871059C>A
CLNSRC
CLNACC RCV000116123.4, RCV000212309.1,