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rs63751022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751022(A;A)
Make rs63751022(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050523
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751022
ebirs63751022
HLIrs63751022
Exacrs63751022
Varsomers63751022
Maprs63751022
PheGenIrs63751022
hapmaprs63751022
1000 genomesrs63751022
hgdprs63751022
ensemblrs63751022
gopubmedrs63751022
geneviewrs63751022
scholarrs63751022
googlers63751022
pharmgkbrs63751022
gwascentralrs63751022
openSNPrs63751022
23andMers63751022
23andMe allrs63751022
SNP Nexus

SNPshotrs63751022
SNPdbers63751022
MSV3drs63751022
GWAS Ctlgrs63751022
Max Magnitude0
ClinVar
Risk rs63751022(A;A)
Alt rs63751022(A;A)
Reference rs63751022(G;G)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37092014G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075553.2, RCV000144606.1, RCV000165669.1,