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rs63751396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751396(-;-)
Make rs63751396(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993617
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63751396
ebirs63751396
HLIrs63751396
Exacrs63751396
Varsomers63751396
Maprs63751396
PheGenIrs63751396
hapmaprs63751396
1000 genomesrs63751396
hgdprs63751396
ensemblrs63751396
gopubmedrs63751396
geneviewrs63751396
scholarrs63751396
googlers63751396
pharmgkbrs63751396
gwascentralrs63751396
openSNPrs63751396
23andMers63751396
23andMe allrs63751396
SNP Nexus

SNPshotrs63751396
SNPdbers63751396
MSV3drs63751396
GWAS Ctlgrs63751396
Max Magnitude0
ClinVar
Risk rs63751396(;)
Alt rs63751396(;)
Reference rs63751396(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035108delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075828.2,