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rs786203700

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203700(A;G)
Make rs786203700(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61857233
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203700
ebirs786203700
HLIrs786203700
Exacrs786203700
Varsomers786203700
Maprs786203700
PheGenIrs786203700
hapmaprs786203700
1000 genomesrs786203700
hgdprs786203700
ensemblrs786203700
gopubmedrs786203700
geneviewrs786203700
scholarrs786203700
googlers786203700
pharmgkbrs786203700
gwascentralrs786203700
openSNPrs786203700
23andMers786203700
23andMe allrs786203700
SNP Nexus

SNPshotrs786203700
SNPdbers786203700
MSV3drs786203700
GWAS Ctlgrs786203700
Max Magnitude0
ClinVar
Risk rs786203700(G;G)
Alt rs786203700(G;G)
Reference rs786203700(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.59934594T>C
CLNSRC
CLNACC RCV000167120.1, RCV000214974.1,