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rs786203898

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203898(A;A)
Make rs786203898(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position61715964
GeneBRIP1
is asnp
is mentioned by
dbSNPrs786203898
ebirs786203898
HLIrs786203898
Exacrs786203898
Varsomers786203898
Maprs786203898
PheGenIrs786203898
hapmaprs786203898
1000 genomesrs786203898
hgdprs786203898
ensemblrs786203898
gopubmedrs786203898
geneviewrs786203898
scholarrs786203898
googlers786203898
pharmgkbrs786203898
gwascentralrs786203898
openSNPrs786203898
23andMers786203898
23andMe allrs786203898
SNP Nexus

SNPshotrs786203898
SNPdbers786203898
MSV3drs786203898
GWAS Ctlgrs786203898
Max Magnitude0
ClinVar
Risk rs786203898(A;A)
Alt rs786203898(A;A)
Reference rs786203898(C;C)
Significance Pathogenic
Disease Familial cancer of breast Fanconi anemia Hereditary cancer-predisposing syndrome
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Fanconi anemia, complementation group J Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.59793325G>A; NC_000017.10:g.59793325G>T
CLNSRC
CLNACC RCV000229009.1, RCV000167402.1,