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rs63750938

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750938(A;A)
Make rs63750938(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017555
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750938
ebirs63750938
HLIrs63750938
Exacrs63750938
Varsomers63750938
Maprs63750938
PheGenIrs63750938
hapmaprs63750938
1000 genomesrs63750938
hgdprs63750938
ensemblrs63750938
gopubmedrs63750938
geneviewrs63750938
scholarrs63750938
googlers63750938
pharmgkbrs63750938
gwascentralrs63750938
openSNPrs63750938
23andMers63750938
23andMe allrs63750938
SNP Nexus

SNPshotrs63750938
SNPdbers63750938
MSV3drs63750938
GWAS Ctlgrs63750938
Max Magnitude0
ClinVar
Risk rs63750938(A;A)
Alt rs63750938(A;A)
Reference rs63750938(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059046T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075882.2,