Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs63751118(-;-)
Make rs63751118(-;GA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025850
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751118
ebirs63751118
HLIrs63751118
Exacrs63751118
Varsomers63751118
Maprs63751118
PheGenIrs63751118
hapmaprs63751118
1000 genomesrs63751118
hgdprs63751118
ensemblrs63751118
gopubmedrs63751118
geneviewrs63751118
scholarrs63751118
googlers63751118
pharmgkbrs63751118
gwascentralrs63751118
openSNPrs63751118
23andMers63751118
23andMe allrs63751118
SNP Nexus

SNPshotrs63751118
SNPdbers63751118
MSV3drs63751118
GWAS Ctlgrs63751118
Max Magnitude0
ClinVar
Risk rs63751118(;)
Alt rs63751118(;)
Reference rs63751118(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067341_37067342delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075159.2,