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rs397509414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509414(-;-)
Make rs397509414(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position52403491
GeneBAP1
is asnp
is mentioned by
dbSNPrs397509414
ebirs397509414
HLIrs397509414
Exacrs397509414
Varsomers397509414
Maprs397509414
PheGenIrs397509414
hapmaprs397509414
1000 genomesrs397509414
hgdprs397509414
ensemblrs397509414
gopubmedrs397509414
geneviewrs397509414
scholarrs397509414
googlers397509414
pharmgkbrs397509414
gwascentralrs397509414
openSNPrs397509414
23andMers397509414
23andMe allrs397509414
SNP Nexus

SNPshotrs397509414
SNPdbers397509414
MSV3drs397509414
GWAS Ctlgrs397509414
Max Magnitude0
ClinVar
Risk rs397509414(;)
Alt rs397509414(;)
Reference rs397509414(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BAP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000003.11:g.52437507delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000049291.3,