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rs63751240

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751240(-;-)
Make rs63751240(-;A)
Make rs63751240(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047599
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751240
ebirs63751240
HLIrs63751240
Exacrs63751240
Varsomers63751240
Maprs63751240
PheGenIrs63751240
hapmaprs63751240
1000 genomesrs63751240
hgdprs63751240
ensemblrs63751240
gopubmedrs63751240
geneviewrs63751240
scholarrs63751240
googlers63751240
pharmgkbrs63751240
gwascentralrs63751240
openSNPrs63751240
23andMers63751240
23andMe allrs63751240
SNP Nexus

SNPshotrs63751240
SNPdbers63751240
MSV3drs63751240
GWAS Ctlgrs63751240
Max Magnitude0
ClinVar
Risk rs63751240(A;A)
Alt rs63751240(A;A)
Reference rs63751240(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089090dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075371.2,