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

rs63750889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750889(A;A)
Make rs63750889(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017566
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750889
ebirs63750889
HLIrs63750889
Exacrs63750889
Varsomers63750889
Maprs63750889
PheGenIrs63750889
hapmaprs63750889
1000 genomesrs63750889
hgdprs63750889
ensemblrs63750889
gopubmedrs63750889
geneviewrs63750889
scholarrs63750889
googlers63750889
pharmgkbrs63750889
gwascentralrs63750889
openSNPrs63750889
23andMers63750889
23andMe allrs63750889
SNP Nexus

SNPshotrs63750889
SNPdbers63750889
MSV3drs63750889
GWAS Ctlgrs63750889
Max Magnitude0
ClinVar
Risk rs63750889(A;A)
Alt rs63750889(A;A)
Reference rs63750889(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059057T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075886.2,