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rs587782726

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Orientationminus
Geno Mag Summary
(TCAA;TCAA) 0 common in clinvar
Make rs587782726(-;-)
Make rs587782726(-;TCAA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61744449
GeneBRIP1, LOC105371851
is asnp
is mentioned by
dbSNPrs587782726
ebirs587782726
HLIrs587782726
Exacrs587782726
Varsomers587782726
Maprs587782726
PheGenIrs587782726
hapmaprs587782726
1000 genomesrs587782726
hgdprs587782726
ensemblrs587782726
gopubmedrs587782726
geneviewrs587782726
scholarrs587782726
googlers587782726
pharmgkbrs587782726
gwascentralrs587782726
openSNPrs587782726
23andMers587782726
23andMe allrs587782726
SNP Nexus

SNPshotrs587782726
SNPdbers587782726
MSV3drs587782726
GWAS Ctlgrs587782726
Max Magnitude0
ClinVar
Risk rs587782726(;)
Alt rs587782726(;)
Reference rs587782726(TCAA;TCAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59821810_59821813delTTGA
CLNSRC
CLNACC RCV000132220.1,