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rs863224525

From SNPedia

Orientationminus
Make rs863224525(-;-)
Make rs863224525(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position61799204
GeneBRIP1
is asnp
is mentioned by
dbSNPrs863224525
ebirs863224525
HLIrs863224525
Exacrs863224525
Varsomers863224525
Maprs863224525
PheGenIrs863224525
hapmaprs863224525
1000 genomesrs863224525
hgdprs863224525
ensemblrs863224525
gopubmedrs863224525
geneviewrs863224525
scholarrs863224525
googlers863224525
pharmgkbrs863224525
gwascentralrs863224525
openSNPrs863224525
23andMers863224525
23andMe allrs863224525
SNP Nexus

SNPshotrs863224525
SNPdbers863224525
MSV3drs863224525
GWAS Ctlgrs863224525
Max Magnitude
ClinVar
Risk rs863224525(;)
Alt rs863224525(;)
Reference rs863224525(A;A)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRIP1
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.59876565delT
CLNSRC
CLNACC RCV000200575.1, RCV000216061.1,