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rs63751701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751701(A;A)
Make rs63751701(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993663
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63751701
ebirs63751701
HLIrs63751701
Exacrs63751701
Varsomers63751701
Maprs63751701
PheGenIrs63751701
hapmaprs63751701
1000 genomesrs63751701
hgdprs63751701
ensemblrs63751701
gopubmedrs63751701
geneviewrs63751701
scholarrs63751701
googlers63751701
pharmgkbrs63751701
gwascentralrs63751701
openSNPrs63751701
23andMers63751701
23andMe allrs63751701
SNP Nexus

SNPshotrs63751701
SNPdbers63751701
MSV3drs63751701
GWAS Ctlgrs63751701
Max Magnitude0
ClinVar
Risk rs63751701(A,T;A,T)
Alt rs63751701(A,T;A,T)
Reference rs63751701(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37035154G>A; NC_000003.11:g.37035154G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075134.2, RCV000202285.1, RCV000075135.2,