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rs63749956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63749956(-;-)
Make rs63749956(-;T)
Make rs63749956(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996652
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749956
ebirs63749956
HLIrs63749956
Exacrs63749956
Varsomers63749956
Maprs63749956
PheGenIrs63749956
hapmaprs63749956
1000 genomesrs63749956
hgdprs63749956
ensemblrs63749956
gopubmedrs63749956
geneviewrs63749956
scholarrs63749956
googlers63749956
pharmgkbrs63749956
gwascentralrs63749956
openSNPrs63749956
23andMers63749956
23andMe allrs63749956
SNP Nexus

SNPshotrs63749956
SNPdbers63749956
MSV3drs63749956
GWAS Ctlgrs63749956
Max Magnitude0
ClinVar
Risk rs63749956(T;T)
Alt rs63749956(T;T)
Reference rs63749956(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038143dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075230.2,