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rs63750891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750891(G;G)
Make rs63750891(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008824
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750891
ebirs63750891
HLIrs63750891
Exacrs63750891
Varsomers63750891
Maprs63750891
PheGenIrs63750891
hapmaprs63750891
1000 genomesrs63750891
hgdprs63750891
ensemblrs63750891
gopubmedrs63750891
geneviewrs63750891
scholarrs63750891
googlers63750891
pharmgkbrs63750891
gwascentralrs63750891
openSNPrs63750891
23andMers63750891
23andMe allrs63750891
SNP Nexus

SNPshotrs63750891
SNPdbers63750891
MSV3drs63750891
GWAS Ctlgrs63750891
Max Magnitude0
ClinVar
Risk rs63750891(G;G)
Alt rs63750891(G;G)
Reference rs63750891(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050315T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075730.2,