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rs63751259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751259(-;-)
Make rs63751259(-;A)
Make rs63751259(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020364
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751259
ebirs63751259
HLIrs63751259
Exacrs63751259
Varsomers63751259
Maprs63751259
PheGenIrs63751259
hapmaprs63751259
1000 genomesrs63751259
hgdprs63751259
ensemblrs63751259
gopubmedrs63751259
geneviewrs63751259
scholarrs63751259
googlers63751259
pharmgkbrs63751259
gwascentralrs63751259
openSNPrs63751259
23andMers63751259
23andMe allrs63751259
SNP Nexus

SNPshotrs63751259
SNPdbers63751259
MSV3drs63751259
GWAS Ctlgrs63751259
Max Magnitude0
ClinVar
Risk rs63751259(A;A)
Alt rs63751259(A;A)
Reference rs63751259(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061855dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075942.2,