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

rs281864938

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864938(-;-)
Make rs281864938(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048566
GeneMLH1
is asnp
is mentioned by
dbSNPrs281864938
ebirs281864938
HLIrs281864938
Exacrs281864938
Varsomers281864938
Maprs281864938
PheGenIrs281864938
hapmaprs281864938
1000 genomesrs281864938
hgdprs281864938
ensemblrs281864938
gopubmedrs281864938
geneviewrs281864938
scholarrs281864938
googlers281864938
pharmgkbrs281864938
gwascentralrs281864938
openSNPrs281864938
23andMers281864938
23andMe allrs281864938
SNP Nexus

SNPshotrs281864938
SNPdbers281864938
MSV3drs281864938
GWAS Ctlgrs281864938
Max Magnitude0
ClinVar
Risk rs281864938(;)
Alt rs281864938(;)
Reference rs281864938(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090057delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075434.2,