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rs786203890

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203890(G;T)
Make rs786203890(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61857088
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203890
ebirs786203890
HLIrs786203890
Exacrs786203890
Varsomers786203890
Maprs786203890
PheGenIrs786203890
hapmaprs786203890
1000 genomesrs786203890
hgdprs786203890
ensemblrs786203890
gopubmedrs786203890
geneviewrs786203890
scholarrs786203890
googlers786203890
pharmgkbrs786203890
gwascentralrs786203890
openSNPrs786203890
23andMers786203890
23andMe allrs786203890
SNP Nexus

SNPshotrs786203890
SNPdbers786203890
MSV3drs786203890
GWAS Ctlgrs786203890
Max Magnitude0
ClinVar
Risk rs786203890(T;T)
Alt rs786203890(T;T)
Reference rs786203890(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59934449C>A
CLNSRC
CLNACC RCV000167391.1,