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rs876658339

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658339(-;-)
Make rs876658339(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37014445
GeneMLH1
is asnp
is mentioned by
dbSNPrs876658339
ebirs876658339
HLIrs876658339
Exacrs876658339
Varsomers876658339
Maprs876658339
PheGenIrs876658339
hapmaprs876658339
1000 genomesrs876658339
hgdprs876658339
ensemblrs876658339
gopubmedrs876658339
geneviewrs876658339
scholarrs876658339
googlers876658339
pharmgkbrs876658339
gwascentralrs876658339
openSNPrs876658339
23andMers876658339
23andMe allrs876658339
SNP Nexus

SNPshotrs876658339
SNPdbers876658339
MSV3drs876658339
GWAS Ctlgrs876658339
Max Magnitude0
ClinVar
Risk rs876658339(;)
Alt rs876658339(;)
Reference rs876658339(A;A)
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.37055936delA
CLNSRC
CLNACC RCV000218228.1,