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rs763443434

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs763443434(-;-)
Make rs763443434(-;AGCTGTCA)
Make rs763443434(AGCTGTCA;AGCTGTCA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61684041
GeneBRIP1
is asnp
is mentioned by
dbSNPrs763443434
ebirs763443434
HLIrs763443434
Exacrs763443434
Varsomers763443434
Maprs763443434
PheGenIrs763443434
hapmaprs763443434
1000 genomesrs763443434
hgdprs763443434
ensemblrs763443434
gopubmedrs763443434
geneviewrs763443434
scholarrs763443434
googlers763443434
pharmgkbrs763443434
gwascentralrs763443434
openSNPrs763443434
23andMers763443434
23andMe allrs763443434
SNP Nexus

SNPshotrs763443434
SNPdbers763443434
MSV3drs763443434
GWAS Ctlgrs763443434
Max Magnitude0
ClinVar
Risk rs763443434(AGCTGTCA;AGCTGTCA)
Alt rs763443434(AGCTGTCA;AGCTGTCA)
Reference rs763443434(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.59761402_59761403insAGCTGTCA
CLNSRC
CLNACC RCV000165914.1,