Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751244(G;T)
Make rs63751244(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042269
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751244
ebirs63751244
HLIrs63751244
Exacrs63751244
Varsomers63751244
Maprs63751244
PheGenIrs63751244
hapmaprs63751244
1000 genomesrs63751244
hgdprs63751244
ensemblrs63751244
gopubmedrs63751244
geneviewrs63751244
scholarrs63751244
googlers63751244
pharmgkbrs63751244
gwascentralrs63751244
openSNPrs63751244
23andMers63751244
23andMe allrs63751244
SNP Nexus

SNPshotrs63751244
SNPdbers63751244
MSV3drs63751244
GWAS Ctlgrs63751244
Max Magnitude0
ClinVar
Risk rs63751244(T;T)
Alt rs63751244(T;T)
Reference rs63751244(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083760G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075308.2,