Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658247

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658247(-;-)
Make rs876658247(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37020395
GeneMLH1
is asnp
is mentioned by
dbSNPrs876658247
ebirs876658247
HLIrs876658247
Exacrs876658247
Varsomers876658247
Maprs876658247
PheGenIrs876658247
hapmaprs876658247
1000 genomesrs876658247
hgdprs876658247
ensemblrs876658247
gopubmedrs876658247
geneviewrs876658247
scholarrs876658247
googlers876658247
pharmgkbrs876658247
gwascentralrs876658247
openSNPrs876658247
23andMers876658247
23andMe allrs876658247
SNP Nexus

SNPshotrs876658247
SNPdbers876658247
MSV3drs876658247
GWAS Ctlgrs876658247
Max Magnitude0
ClinVar
Risk rs876658247(;)
Alt rs876658247(;)
Reference rs876658247(G;G)
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.37061886delG
CLNSRC
CLNACC RCV000220801.1,