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

rs63750281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750281(A;A)
Make rs63750281(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996705
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750281
ebirs63750281
HLIrs63750281
Exacrs63750281
Varsomers63750281
Maprs63750281
PheGenIrs63750281
hapmaprs63750281
1000 genomesrs63750281
hgdprs63750281
ensemblrs63750281
gopubmedrs63750281
geneviewrs63750281
scholarrs63750281
googlers63750281
pharmgkbrs63750281
gwascentralrs63750281
openSNPrs63750281
23andMers63750281
23andMe allrs63750281
SNP Nexus

SNPshotrs63750281
SNPdbers63750281
MSV3drs63750281
GWAS Ctlgrs63750281
Max Magnitude0
ClinVar
Risk rs63750281(A;A)
Alt rs63750281(A;A)
Reference rs63750281(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038196T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075492.2,