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rs863224525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224525(-;-)
Make rs863224525(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61799204
GeneBRIP1
is asnp
is mentioned by
dbSNPrs863224525
dbSNP (old)rs863224525
ClinGenrs863224525
ebirs863224525
HLIrs863224525
Exacrs863224525
Gnomadrs863224525
Varsomers863224525
Maprs863224525
PheGenIrs863224525
Biobankrs863224525
1000 genomesrs863224525
hgdprs863224525
ensemblrs863224525
gopubmedrs863224525
geneviewrs863224525
scholarrs863224525
googlers863224525
pharmgkbrs863224525
gwascentralrs863224525
openSNPrs863224525
23andMers863224525
23andMe allrs863224525
SNP Nexus

SNPshotrs863224525
SNPdbers863224525
MSV3drs863224525
GWAS Ctlgrs863224525
Max Magnitude0
ClinVar
Risk rs863224525(-;-)
Alt rs863224525(-;-)
Reference Rs863224525(A;A)
Significance Pathogenic
Disease Familial cancer of breast Fanconi anemia Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Fanconi anemia, complementation group J Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.59876565delT
CLNSRC
CLNACC RCV000200575.2, RCV000216061.1, RCV000481091.1,