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rs752309409

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752309409(A;A)
Make rs752309409(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61808634
GeneBRIP1
is asnp
is mentioned by
dbSNPrs752309409
ebirs752309409
HLIrs752309409
Exacrs752309409
Varsomers752309409
Maprs752309409
PheGenIrs752309409
hapmaprs752309409
1000 genomesrs752309409
hgdprs752309409
ensemblrs752309409
gopubmedrs752309409
geneviewrs752309409
scholarrs752309409
googlers752309409
pharmgkbrs752309409
gwascentralrs752309409
openSNPrs752309409
23andMers752309409
23andMe allrs752309409
SNP Nexus

SNPshotrs752309409
SNPdbers752309409
MSV3drs752309409
GWAS Ctlgrs752309409
Max Magnitude0
ClinVar
Risk rs752309409(A;A)
Alt rs752309409(A;A)
Reference rs752309409(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 0
HGVS NC_000017.10:g.59885995G>A
CLNSRC
CLNACC RCV000165345.1, RCV000206065.1, RCV000219928.1,