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

rs63750726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750726(C;T)
Make rs63750726(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048581
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750726
ebirs63750726
HLIrs63750726
Exacrs63750726
Varsomers63750726
Maprs63750726
PheGenIrs63750726
hapmaprs63750726
1000 genomesrs63750726
hgdprs63750726
ensemblrs63750726
gopubmedrs63750726
geneviewrs63750726
scholarrs63750726
googlers63750726
pharmgkbrs63750726
gwascentralrs63750726
openSNPrs63750726
23andMers63750726
23andMe allrs63750726
SNP Nexus

SNPshotrs63750726
SNPdbers63750726
MSV3drs63750726
GWAS Ctlgrs63750726
Max Magnitude0
ClinVar
Risk rs63750726(T;T)
Alt rs63750726(T;T)
Reference rs63750726(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37090072C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075439.2, RCV000215855.1,