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rs63749950

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749950(C;T)
Make rs63749950(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017557
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749950
ebirs63749950
HLIrs63749950
Exacrs63749950
Varsomers63749950
Maprs63749950
PheGenIrs63749950
hapmaprs63749950
1000 genomesrs63749950
hgdprs63749950
ensemblrs63749950
gopubmedrs63749950
geneviewrs63749950
scholarrs63749950
googlers63749950
pharmgkbrs63749950
gwascentralrs63749950
openSNPrs63749950
23andMers63749950
23andMe allrs63749950
SNP Nexus

SNPshotrs63749950
SNPdbers63749950
MSV3drs63749950
GWAS Ctlgrs63749950
Max Magnitude0
ClinVar
Risk rs63749950(T;T)
Alt rs63749950(T;T)
Reference rs63749950(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059048C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075883.2,