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rs63749837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749837(-;-)
Make rs63749837(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020448
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749837
ebirs63749837
HLIrs63749837
Exacrs63749837
Varsomers63749837
Maprs63749837
PheGenIrs63749837
hapmaprs63749837
1000 genomesrs63749837
hgdprs63749837
ensemblrs63749837
gopubmedrs63749837
geneviewrs63749837
scholarrs63749837
googlers63749837
pharmgkbrs63749837
gwascentralrs63749837
openSNPrs63749837
23andMers63749837
23andMe allrs63749837
SNP Nexus

SNPshotrs63749837
SNPdbers63749837
MSV3drs63749837
GWAS Ctlgrs63749837
Max Magnitude0
ClinVar
Risk rs63749837(;)
Alt rs63749837(;)
Reference rs63749837(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061939delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075076.2,