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rs63749926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749926(-;-)
Make rs63749926(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020379
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749926
ebirs63749926
HLIrs63749926
Exacrs63749926
Varsomers63749926
Maprs63749926
PheGenIrs63749926
hapmaprs63749926
1000 genomesrs63749926
hgdprs63749926
ensemblrs63749926
gopubmedrs63749926
geneviewrs63749926
scholarrs63749926
googlers63749926
pharmgkbrs63749926
gwascentralrs63749926
openSNPrs63749926
23andMers63749926
23andMe allrs63749926
SNP Nexus

SNPshotrs63749926
SNPdbers63749926
MSV3drs63749926
GWAS Ctlgrs63749926
Max Magnitude0
ClinVar
Risk rs63749926(;)
Alt rs63749926(;)
Reference rs63749926(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061870delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075944.2,