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rs786202610

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202610(-;-)
Make rs786202610(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61808495
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786202610
dbSNP (old)rs786202610
ClinGenrs786202610
ebirs786202610
HLIrs786202610
Exacrs786202610
Gnomadrs786202610
Varsomers786202610
Maprs786202610
PheGenIrs786202610
Biobankrs786202610
1000 genomesrs786202610
hgdprs786202610
ensemblrs786202610
gopubmedrs786202610
geneviewrs786202610
scholarrs786202610
googlers786202610
pharmgkbrs786202610
gwascentralrs786202610
openSNPrs786202610
23andMers786202610
23andMe allrs786202610
SNP Nexus

SNPshotrs786202610
SNPdbers786202610
MSV3drs786202610
GWAS Ctlgrs786202610
Max Magnitude0
ClinVar
Risk rs786202610(-;-)
Alt rs786202610(-;-)
Reference Rs786202610(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided
Reversed 1
HGVS NC_000017.10:g.59885856delT
CLNSRC
CLNACC RCV000165504.1, RCV000168341.3, RCV000481880.1,