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rs63749820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749820(C;T)
Make rs63749820(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007046
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749820
ebirs63749820
HLIrs63749820
Exacrs63749820
Varsomers63749820
Maprs63749820
PheGenIrs63749820
hapmaprs63749820
1000 genomesrs63749820
hgdprs63749820
ensemblrs63749820
gopubmedrs63749820
geneviewrs63749820
scholarrs63749820
googlers63749820
pharmgkbrs63749820
gwascentralrs63749820
openSNPrs63749820
23andMers63749820
23andMe allrs63749820
SNP Nexus

SNPshotrs63749820
SNPdbers63749820
MSV3drs63749820
GWAS Ctlgrs63749820
Max Magnitude0
ClinVar
Risk rs63749820(T;T)
Alt rs63749820(T;T)
Reference rs63749820(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048537C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075706.2,