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rs747604569

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747604569(A;A)
Make rs747604569(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61849152
GeneBRIP1
is asnp
is mentioned by
dbSNPrs747604569
ebirs747604569
HLIrs747604569
Exacrs747604569
Varsomers747604569
Maprs747604569
PheGenIrs747604569
hapmaprs747604569
1000 genomesrs747604569
hgdprs747604569
ensemblrs747604569
gopubmedrs747604569
geneviewrs747604569
scholarrs747604569
googlers747604569
pharmgkbrs747604569
gwascentralrs747604569
openSNPrs747604569
23andMers747604569
23andMe allrs747604569
SNP Nexus

SNPshotrs747604569
SNPdbers747604569
MSV3drs747604569
GWAS Ctlgrs747604569
Max Magnitude0
ClinVar
Risk rs747604569(A;A)
Alt rs747604569(A;A)
Reference rs747604569(G;G)
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.59926513G>A
CLNSRC
CLNACC RCV000166003.1, RCV000198978.1,