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rs63751711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751711(A;A)
Make rs63751711(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012099
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751711
ebirs63751711
HLIrs63751711
Exacrs63751711
Varsomers63751711
Maprs63751711
PheGenIrs63751711
hapmaprs63751711
1000 genomesrs63751711
hgdprs63751711
ensemblrs63751711
gopubmedrs63751711
geneviewrs63751711
scholarrs63751711
googlers63751711
pharmgkbrs63751711
gwascentralrs63751711
openSNPrs63751711
23andMers63751711
23andMe allrs63751711
SNP Nexus

SNPshotrs63751711
SNPdbers63751711
MSV3drs63751711
GWAS Ctlgrs63751711
Max Magnitude0
ClinVar
Risk rs63751711(A,T;A,T)
Alt rs63751711(A,T;A,T)
Reference rs63751711(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37053590G>A; NC_000003.11:g.37053590G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075809.2, RCV000132197.2, RCV000202049.1, RCV000075810.3, RCV000160555.2,