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rs63751657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751657(A;A)
Make rs63751657(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042331
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751657
ebirs63751657
HLIrs63751657
Exacrs63751657
Varsomers63751657
Maprs63751657
PheGenIrs63751657
hapmaprs63751657
1000 genomesrs63751657
hgdprs63751657
ensemblrs63751657
gopubmedrs63751657
geneviewrs63751657
scholarrs63751657
googlers63751657
pharmgkbrs63751657
gwascentralrs63751657
openSNPrs63751657
23andMers63751657
23andMe allrs63751657
SNP Nexus

SNPshotrs63751657
SNPdbers63751657
MSV3drs63751657
GWAS Ctlgrs63751657
Max Magnitude0
ClinVar
Risk rs63751657(A,C;A,C)
Alt rs63751657(A,C;A,C)
Reference rs63751657(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37083822G>A; NC_000003.11:g.37083822G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075331.2, RCV000132025.3, RCV000202231.1, RCV000075332.2,