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rs63749944

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749944(-;-)
Make rs63749944(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008873
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749944
ebirs63749944
HLIrs63749944
Exacrs63749944
Varsomers63749944
Maprs63749944
PheGenIrs63749944
hapmaprs63749944
1000 genomesrs63749944
hgdprs63749944
ensemblrs63749944
gopubmedrs63749944
geneviewrs63749944
scholarrs63749944
googlers63749944
pharmgkbrs63749944
gwascentralrs63749944
openSNPrs63749944
23andMers63749944
23andMe allrs63749944
SNP Nexus

SNPshotrs63749944
SNPdbers63749944
MSV3drs63749944
GWAS Ctlgrs63749944
Max Magnitude0
ClinVar
Risk rs63749944(;)
Alt rs63749944(;)
Reference rs63749944(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050364delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075741.2,