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rs786204250

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204250(A;A)
Make rs786204250(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61715996
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786204250
ebirs786204250
HLIrs786204250
Exacrs786204250
Varsomers786204250
Maprs786204250
PheGenIrs786204250
hapmaprs786204250
1000 genomesrs786204250
hgdprs786204250
ensemblrs786204250
gopubmedrs786204250
geneviewrs786204250
scholarrs786204250
googlers786204250
pharmgkbrs786204250
gwascentralrs786204250
openSNPrs786204250
23andMers786204250
23andMe allrs786204250
SNP Nexus

SNPshotrs786204250
SNPdbers786204250
MSV3drs786204250
GWAS Ctlgrs786204250
Max Magnitude0
ClinVar
Risk rs786204250(A;A)
Alt rs786204250(A;A)
Reference rs786204250(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.59793357C>T
CLNSRC
CLNACC RCV000168450.2,