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rs281864937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs281864937(-;-)
Make rs281864937(-;GA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028789
GeneMLH1
is asnp
is mentioned by
dbSNPrs281864937
ebirs281864937
HLIrs281864937
Exacrs281864937
Varsomers281864937
Maprs281864937
PheGenIrs281864937
hapmaprs281864937
1000 genomesrs281864937
hgdprs281864937
ensemblrs281864937
gopubmedrs281864937
geneviewrs281864937
scholarrs281864937
googlers281864937
pharmgkbrs281864937
gwascentralrs281864937
openSNPrs281864937
23andMers281864937
23andMe allrs281864937
SNP Nexus

SNPshotrs281864937
SNPdbers281864937
MSV3drs281864937
GWAS Ctlgrs281864937
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs281864937(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070280_37070281delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075207.2,