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rs72481822

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72481822(A;A)
Make rs72481822(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position36993550
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs72481822
ebirs72481822
HLIrs72481822
Exacrs72481822
Varsomers72481822
Maprs72481822
PheGenIrs72481822
hapmaprs72481822
1000 genomesrs72481822
hgdprs72481822
ensemblrs72481822
gopubmedrs72481822
geneviewrs72481822
scholarrs72481822
googlers72481822
pharmgkbrs72481822
gwascentralrs72481822
openSNPrs72481822
23andMers72481822
23andMe allrs72481822
SNP Nexus

SNPshotrs72481822
SNPdbers72481822
MSV3drs72481822
GWAS Ctlgrs72481822
Max Magnitude0
ClinVar
Risk rs72481822(A;A)
Alt rs72481822(A;A)
Reference rs72481822(G;G)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37035041G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075700.2, RCV000215403.1,