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rs876659226

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659226(-;-)
Make rs876659226(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37025688
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659226
ebirs876659226
HLIrs876659226
Exacrs876659226
Varsomers876659226
Maprs876659226
PheGenIrs876659226
hapmaprs876659226
1000 genomesrs876659226
hgdprs876659226
ensemblrs876659226
gopubmedrs876659226
geneviewrs876659226
scholarrs876659226
googlers876659226
pharmgkbrs876659226
gwascentralrs876659226
openSNPrs876659226
23andMers876659226
23andMe allrs876659226
SNP Nexus

SNPshotrs876659226
SNPdbers876659226
MSV3drs876659226
GWAS Ctlgrs876659226
Max Magnitude0
ClinVar
Risk rs876659226(;)
Alt rs876659226(;)
Reference rs876659226(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.37067179delA
CLNSRC
CLNACC RCV000214230.1,