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rs63751637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs63751637(-;-)
Make rs63751637(-;GA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012019
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751637
ebirs63751637
HLIrs63751637
Exacrs63751637
Varsomers63751637
Maprs63751637
PheGenIrs63751637
hapmaprs63751637
1000 genomesrs63751637
hgdprs63751637
ensemblrs63751637
gopubmedrs63751637
geneviewrs63751637
scholarrs63751637
googlers63751637
pharmgkbrs63751637
gwascentralrs63751637
openSNPrs63751637
23andMers63751637
23andMe allrs63751637
SNP Nexus

SNPshotrs63751637
SNPdbers63751637
MSV3drs63751637
GWAS Ctlgrs63751637
Max Magnitude0
ClinVar
Risk rs63751637(;)
Alt rs63751637(;)
Reference rs63751637(GA;GA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053510_37053511delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075783.2,