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rs63751045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751045(-;-)
Make rs63751045(-;C)
Make rs63751045(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007038
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751045
ebirs63751045
HLIrs63751045
Exacrs63751045
Varsomers63751045
Maprs63751045
PheGenIrs63751045
hapmaprs63751045
1000 genomesrs63751045
hgdprs63751045
ensemblrs63751045
gopubmedrs63751045
geneviewrs63751045
scholarrs63751045
googlers63751045
pharmgkbrs63751045
gwascentralrs63751045
openSNPrs63751045
23andMers63751045
23andMe allrs63751045
SNP Nexus

SNPshotrs63751045
SNPdbers63751045
MSV3drs63751045
GWAS Ctlgrs63751045
Max Magnitude0
ClinVar
Risk rs63751045(C;C)
Alt rs63751045(C;C)
Reference rs63751045(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048529dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075705.2,