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rs63749981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63749981(-;-)
Make rs63749981(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025941
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749981
ebirs63749981
HLIrs63749981
Exacrs63749981
Varsomers63749981
Maprs63749981
PheGenIrs63749981
hapmaprs63749981
1000 genomesrs63749981
hgdprs63749981
ensemblrs63749981
gopubmedrs63749981
geneviewrs63749981
scholarrs63749981
googlers63749981
pharmgkbrs63749981
gwascentralrs63749981
openSNPrs63749981
23andMers63749981
23andMe allrs63749981
SNP Nexus

SNPshotrs63749981
SNPdbers63749981
MSV3drs63749981
GWAS Ctlgrs63749981
Max Magnitude0
ClinVar
Risk rs63749981(;)
Alt rs63749981(;)
Reference rs63749981(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067432delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075175.2,