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rs63751124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751124(G;T)
Make rs63751124(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007007
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751124
ebirs63751124
HLIrs63751124
Exacrs63751124
Varsomers63751124
Maprs63751124
PheGenIrs63751124
hapmaprs63751124
1000 genomesrs63751124
hgdprs63751124
ensemblrs63751124
gopubmedrs63751124
geneviewrs63751124
scholarrs63751124
googlers63751124
pharmgkbrs63751124
gwascentralrs63751124
openSNPrs63751124
23andMers63751124
23andMe allrs63751124
SNP Nexus

SNPshotrs63751124
SNPdbers63751124
MSV3drs63751124
GWAS Ctlgrs63751124
Max Magnitude0
ClinVar
Risk rs63751124(T;T)
Alt rs63751124(T;T)
Reference rs63751124(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048498G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075698.2,