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rs63751472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751472(G;T)
Make rs63751472(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028908
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751472
ebirs63751472
HLIrs63751472
Exacrs63751472
Varsomers63751472
Maprs63751472
PheGenIrs63751472
hapmaprs63751472
1000 genomesrs63751472
hgdprs63751472
ensemblrs63751472
gopubmedrs63751472
geneviewrs63751472
scholarrs63751472
googlers63751472
pharmgkbrs63751472
gwascentralrs63751472
openSNPrs63751472
23andMers63751472
23andMe allrs63751472
SNP Nexus

SNPshotrs63751472
SNPdbers63751472
MSV3drs63751472
GWAS Ctlgrs63751472
Max Magnitude0
ClinVar
Risk rs63751472(T;T)
Alt rs63751472(T;T)
Reference rs63751472(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070399G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075236.2,