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rs63751598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751598(A;G)
Make rs63751598(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017598
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751598
ebirs63751598
HLIrs63751598
Exacrs63751598
Varsomers63751598
Maprs63751598
PheGenIrs63751598
hapmaprs63751598
1000 genomesrs63751598
hgdprs63751598
ensemblrs63751598
gopubmedrs63751598
geneviewrs63751598
scholarrs63751598
googlers63751598
pharmgkbrs63751598
gwascentralrs63751598
openSNPrs63751598
23andMers63751598
23andMe allrs63751598
SNP Nexus

SNPshotrs63751598
SNPdbers63751598
MSV3drs63751598
GWAS Ctlgrs63751598
Max Magnitude0
ClinVar
Risk rs63751598(C,G;C,G)
Alt rs63751598(C,G;C,G)
Reference rs63751598(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059089A>C; NC_000003.11:g.37059089A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075901.2, RCV000075902.2,