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rs63750098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750098(A;A)
Make rs63750098(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996648
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750098
ebirs63750098
HLIrs63750098
Exacrs63750098
Varsomers63750098
Maprs63750098
PheGenIrs63750098
hapmaprs63750098
1000 genomesrs63750098
hgdprs63750098
ensemblrs63750098
gopubmedrs63750098
geneviewrs63750098
scholarrs63750098
googlers63750098
pharmgkbrs63750098
gwascentralrs63750098
openSNPrs63750098
23andMers63750098
23andMe allrs63750098
SNP Nexus

SNPshotrs63750098
SNPdbers63750098
MSV3drs63750098
GWAS Ctlgrs63750098
Max Magnitude0
ClinVar
Risk rs63750098(A;A)
Alt rs63750098(A;A)
Reference rs63750098(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038139T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075223.2,