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rs63751283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751283(G;G)
Make rs63751283(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014533
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751283
ebirs63751283
HLIrs63751283
Exacrs63751283
Varsomers63751283
Maprs63751283
PheGenIrs63751283
hapmaprs63751283
1000 genomesrs63751283
hgdprs63751283
ensemblrs63751283
gopubmedrs63751283
geneviewrs63751283
scholarrs63751283
googlers63751283
pharmgkbrs63751283
gwascentralrs63751283
openSNPrs63751283
23andMers63751283
23andMe allrs63751283
SNP Nexus

SNPshotrs63751283
SNPdbers63751283
MSV3drs63751283
GWAS Ctlgrs63751283
Max Magnitude0
ClinVar
Risk rs63751283(G;G)
Alt rs63751283(G;G)
Reference rs63751283(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37056024T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075841.2,