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rs876660073

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660073(A;A)
Make rs876660073(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position65076639
GeneMAX
is asnp
is mentioned by
dbSNPrs876660073
ebirs876660073
HLIrs876660073
Exacrs876660073
Varsomers876660073
Maprs876660073
PheGenIrs876660073
hapmaprs876660073
1000 genomesrs876660073
hgdprs876660073
ensemblrs876660073
gopubmedrs876660073
geneviewrs876660073
scholarrs876660073
googlers876660073
pharmgkbrs876660073
gwascentralrs876660073
openSNPrs876660073
23andMers876660073
23andMe allrs876660073
SNP Nexus

SNPshotrs876660073
SNPdbers876660073
MSV3drs876660073
GWAS Ctlgrs876660073
Max Magnitude0
ClinVar
Risk rs876660073(A;A)
Alt rs876660073(A;A)
Reference rs876660073(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MAX
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000014.8:g.65543357G>T
CLNSRC
CLNACC RCV000218866.1,