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rs587780224

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587780224(-;-)
Make rs587780224(-;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61801266
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587780224
ebirs587780224
HLIrs587780224
Exacrs587780224
Varsomers587780224
Maprs587780224
PheGenIrs587780224
hapmaprs587780224
1000 genomesrs587780224
hgdprs587780224
ensemblrs587780224
gopubmedrs587780224
geneviewrs587780224
scholarrs587780224
googlers587780224
pharmgkbrs587780224
gwascentralrs587780224
openSNPrs587780224
23andMers587780224
23andMe allrs587780224
SNP Nexus

SNPshotrs587780224
SNPdbers587780224
MSV3drs587780224
GWAS Ctlgrs587780224
Max Magnitude0
ClinVar
Risk rs587780224(;)
Alt rs587780224(;)
Reference rs587780224(CA;CA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59878627_59878628delTG
CLNSRC
CLNACC RCV000116118.4,