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rs786202941

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202941(C;C)
Make rs786202941(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61776400
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786202941
ebirs786202941
HLIrs786202941
Exacrs786202941
Varsomers786202941
Maprs786202941
PheGenIrs786202941
hapmaprs786202941
1000 genomesrs786202941
hgdprs786202941
ensemblrs786202941
gopubmedrs786202941
geneviewrs786202941
scholarrs786202941
googlers786202941
pharmgkbrs786202941
gwascentralrs786202941
openSNPrs786202941
23andMers786202941
23andMe allrs786202941
SNP Nexus

SNPshotrs786202941
SNPdbers786202941
MSV3drs786202941
GWAS Ctlgrs786202941
Max Magnitude0
ClinVar
Risk rs786202941(C;C)
Alt rs786202941(C;C)
Reference rs786202941(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59853761C>G
CLNSRC
CLNACC RCV000166016.1,