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rs63749845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749845(-;-)
Make rs63749845(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025932
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749845
ebirs63749845
HLIrs63749845
Exacrs63749845
Varsomers63749845
Maprs63749845
PheGenIrs63749845
hapmaprs63749845
1000 genomesrs63749845
hgdprs63749845
ensemblrs63749845
gopubmedrs63749845
geneviewrs63749845
scholarrs63749845
googlers63749845
pharmgkbrs63749845
gwascentralrs63749845
openSNPrs63749845
23andMers63749845
23andMe allrs63749845
SNP Nexus

SNPshotrs63749845
SNPdbers63749845
MSV3drs63749845
GWAS Ctlgrs63749845
Max Magnitude0
ClinVar
Risk rs63749845(;)
Alt rs63749845(;)
Reference rs63749845(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067423delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075173.2,