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rs786203384

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203384(A;TCC)
Make rs786203384(TCC;TCC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61744581
GeneBRIP1, LOC105371851
is asnp
is mentioned by
dbSNPrs786203384
ebirs786203384
HLIrs786203384
Exacrs786203384
Varsomers786203384
Maprs786203384
PheGenIrs786203384
hapmaprs786203384
1000 genomesrs786203384
hgdprs786203384
ensemblrs786203384
gopubmedrs786203384
geneviewrs786203384
scholarrs786203384
googlers786203384
pharmgkbrs786203384
gwascentralrs786203384
openSNPrs786203384
23andMers786203384
23andMe allrs786203384
SNP Nexus

SNPshotrs786203384
SNPdbers786203384
MSV3drs786203384
GWAS Ctlgrs786203384
Max Magnitude0
ClinVar
Risk rs786203384(TCC;TCC)
Alt rs786203384(TCC;TCC)
Reference rs786203384(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.59821942delTinsGGA
CLNSRC
CLNACC RCV000166665.1, RCV000203877.1,