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rs863224479

From SNPedia

Merged intors267607898
Orientationplus
Stabilizedplus
Geno Mag Summary
(CACA;CACA) 0 common in clinvar
Make rs863224479(-;-)
Make rs863224479(-;CACA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37050559
GeneMLH1
is asnp
is mentioned by
dbSNPrs863224479
dbSNP (old)rs863224479
ClinGenrs863224479
ebirs863224479
HLIrs863224479
Exacrs863224479
Gnomadrs863224479
Varsomers863224479
Maprs863224479
PheGenIrs863224479
Biobankrs863224479
1000 genomesrs863224479
hgdprs863224479
ensemblrs863224479
gopubmedrs863224479
geneviewrs863224479
scholarrs863224479
googlers863224479
pharmgkbrs863224479
gwascentralrs863224479
openSNPrs863224479
23andMers863224479
23andMe allrs863224479
SNP Nexus

SNPshotrs863224479
SNPdbers863224479
MSV3drs863224479
GWAS Ctlgrs863224479
StatusMerged into rs267607898
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863224479(CACA;CACA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37092052_37092055delCACA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075569.2, RCV000164558.2, RCV000202306.2,