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rs63750192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750192(C;T)
Make rs63750192(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040251
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750192
ebirs63750192
HLIrs63750192
Exacrs63750192
Varsomers63750192
Maprs63750192
PheGenIrs63750192
hapmaprs63750192
1000 genomesrs63750192
hgdprs63750192
ensemblrs63750192
gopubmedrs63750192
geneviewrs63750192
scholarrs63750192
googlers63750192
pharmgkbrs63750192
gwascentralrs63750192
openSNPrs63750192
23andMers63750192
23andMe allrs63750192
SNP Nexus

SNPshotrs63750192
SNPdbers63750192
MSV3drs63750192
GWAS Ctlgrs63750192
Max Magnitude0
ClinVar
Risk rs63750192(T;T)
Alt rs63750192(T;T)
Reference rs63750192(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081742C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075283.3,