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rs63751677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751677(-;-)
Make rs63751677(-;A)
Make rs63751677(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028786
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751677
ebirs63751677
HLIrs63751677
Exacrs63751677
Varsomers63751677
Maprs63751677
PheGenIrs63751677
hapmaprs63751677
1000 genomesrs63751677
hgdprs63751677
ensemblrs63751677
gopubmedrs63751677
geneviewrs63751677
scholarrs63751677
googlers63751677
pharmgkbrs63751677
gwascentralrs63751677
openSNPrs63751677
23andMers63751677
23andMe allrs63751677
SNP Nexus

SNPshotrs63751677
SNPdbers63751677
MSV3drs63751677
GWAS Ctlgrs63751677
Max Magnitude0
ClinVar
Risk rs63751677(A;A)
Alt rs63751677(A;A)
Reference rs63751677(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070277dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075202.2,