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rs763009188

From SNPedia

Orientationplus
Geno Mag Summary
(TTGT;TTGT) 0 common in clinvar
Make rs763009188(-;-)
Make rs763009188(-;TTGT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61857144
GeneBRIP1
is asnp
is mentioned by
dbSNPrs763009188
ebirs763009188
HLIrs763009188
Exacrs763009188
Varsomers763009188
Maprs763009188
PheGenIrs763009188
hapmaprs763009188
1000 genomesrs763009188
hgdprs763009188
ensemblrs763009188
gopubmedrs763009188
geneviewrs763009188
scholarrs763009188
googlers763009188
pharmgkbrs763009188
gwascentralrs763009188
openSNPrs763009188
23andMers763009188
23andMe allrs763009188
SNP Nexus

SNPshotrs763009188
SNPdbers763009188
MSV3drs763009188
GWAS Ctlgrs763009188
Max Magnitude0
ClinVar
Risk rs763009188(;)
Alt rs763009188(;)
Reference rs763009188(TTGT;TTGT)
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 0
HGVS NC_000017.10:g.59934505_59934508delTTGT
CLNSRC
CLNACC RCV000167103.1, RCV000197800.2,