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rs876658821

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs876658821(-;-)
Make rs876658821(-;AG)
Make rs876658821(AG;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37028896
GeneMLH1
is asnp
is mentioned by
dbSNPrs876658821
ebirs876658821
HLIrs876658821
Exacrs876658821
Varsomers876658821
Maprs876658821
PheGenIrs876658821
hapmaprs876658821
1000 genomesrs876658821
hgdprs876658821
ensemblrs876658821
gopubmedrs876658821
geneviewrs876658821
scholarrs876658821
googlers876658821
pharmgkbrs876658821
gwascentralrs876658821
openSNPrs876658821
23andMers876658821
23andMe allrs876658821
SNP Nexus

SNPshotrs876658821
SNPdbers876658821
MSV3drs876658821
GWAS Ctlgrs876658821
Max Magnitude0
ClinVar
Risk rs876658821(;)
Alt rs876658821(;)
Reference rs876658821(GA;GA)
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.37070387_37070388delAG
CLNSRC
CLNACC RCV000218055.1,