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rs786201808

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201808(A;A)
Make rs786201808(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61801388
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786201808
ebirs786201808
HLIrs786201808
Exacrs786201808
Varsomers786201808
Maprs786201808
PheGenIrs786201808
hapmaprs786201808
1000 genomesrs786201808
hgdprs786201808
ensemblrs786201808
gopubmedrs786201808
geneviewrs786201808
scholarrs786201808
googlers786201808
pharmgkbrs786201808
gwascentralrs786201808
openSNPrs786201808
23andMers786201808
23andMe allrs786201808
SNP Nexus

SNPshotrs786201808
SNPdbers786201808
MSV3drs786201808
GWAS Ctlgrs786201808
Max Magnitude0
ClinVar
Risk rs786201808(A;A)
Alt rs786201808(A;A)
Reference rs786201808(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.59878749C>T
CLNSRC
CLNACC RCV000164287.1,