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

rs63750489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750489(C;T)
Make rs63750489(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020326
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750489
ebirs63750489
HLIrs63750489
Exacrs63750489
Varsomers63750489
Maprs63750489
PheGenIrs63750489
hapmaprs63750489
1000 genomesrs63750489
hgdprs63750489
ensemblrs63750489
gopubmedrs63750489
geneviewrs63750489
scholarrs63750489
googlers63750489
pharmgkbrs63750489
gwascentralrs63750489
openSNPrs63750489
23andMers63750489
23andMe allrs63750489
SNP Nexus

SNPshotrs63750489
SNPdbers63750489
MSV3drs63750489
GWAS Ctlgrs63750489
Max Magnitude0
ClinVar
Risk rs63750489(T;T)
Alt rs63750489(T;T)
Reference rs63750489(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061817C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075928.3,