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

rs63750484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750484(A;A)
Make rs63750484(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050545
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750484
ebirs63750484
HLIrs63750484
Exacrs63750484
Varsomers63750484
Maprs63750484
PheGenIrs63750484
hapmaprs63750484
1000 genomesrs63750484
hgdprs63750484
ensemblrs63750484
gopubmedrs63750484
geneviewrs63750484
scholarrs63750484
googlers63750484
pharmgkbrs63750484
gwascentralrs63750484
openSNPrs63750484
23andMers63750484
23andMe allrs63750484
SNP Nexus

SNPshotrs63750484
SNPdbers63750484
MSV3drs63750484
GWAS Ctlgrs63750484
Max Magnitude0
ClinVar
Risk rs63750484(A;A)
Alt rs63750484(A;A)
Reference rs63750484(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092036T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075565.2,