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rs869025212

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025212(-;-)
Make rs869025212(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position52403428
GeneBAP1
is asnp
is mentioned by
dbSNPrs869025212
ebirs869025212
HLIrs869025212
Exacrs869025212
Varsomers869025212
Maprs869025212
PheGenIrs869025212
hapmaprs869025212
1000 genomesrs869025212
hgdprs869025212
ensemblrs869025212
gopubmedrs869025212
geneviewrs869025212
scholarrs869025212
googlers869025212
pharmgkbrs869025212
gwascentralrs869025212
openSNPrs869025212
23andMers869025212
23andMe allrs869025212
SNP Nexus

SNPshotrs869025212
SNPdbers869025212
MSV3drs869025212
GWAS Ctlgrs869025212
Max Magnitude0
ClinVar
Risk rs869025212(;)
Alt rs869025212(;)
Reference rs869025212(C;C)
Significance Pathogenic
Disease BAP1 Cancer Syndrome
Variation info
Gene BAP1
CLNDBN BAP1 Cancer Syndrome
Reversed 1
HGVS NC_000003.11:g.52437444delG
CLNSRC
CLNACC RCV000207031.1,