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rs876660589

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660589(-;-)
Make rs876660589(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37040283
GeneMLH1
is asnp
is mentioned by
dbSNPrs876660589
ebirs876660589
HLIrs876660589
Exacrs876660589
Varsomers876660589
Maprs876660589
PheGenIrs876660589
hapmaprs876660589
1000 genomesrs876660589
hgdprs876660589
ensemblrs876660589
gopubmedrs876660589
geneviewrs876660589
scholarrs876660589
googlers876660589
pharmgkbrs876660589
gwascentralrs876660589
openSNPrs876660589
23andMers876660589
23andMe allrs876660589
SNP Nexus

SNPshotrs876660589
SNPdbers876660589
MSV3drs876660589
GWAS Ctlgrs876660589
Max Magnitude0
ClinVar
Risk rs876660589(;)
Alt rs876660589(;)
Reference rs876660589(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37081774delC
CLNSRC
CLNACC RCV000219180.1,