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rs63751707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751707(C;T)
Make rs63751707(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017597
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751707
ebirs63751707
HLIrs63751707
Exacrs63751707
Varsomers63751707
Maprs63751707
PheGenIrs63751707
hapmaprs63751707
1000 genomesrs63751707
hgdprs63751707
ensemblrs63751707
gopubmedrs63751707
geneviewrs63751707
scholarrs63751707
googlers63751707
pharmgkbrs63751707
gwascentralrs63751707
openSNPrs63751707
23andMers63751707
23andMe allrs63751707
SNP Nexus

SNPshotrs63751707
SNPdbers63751707
MSV3drs63751707
GWAS Ctlgrs63751707
Max Magnitude0
ClinVar
Risk rs63751707(G,T;G,T)
Alt rs63751707(G,T;G,T)
Reference rs63751707(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059088C>G; NC_000003.11:g.37059088C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075899.2, RCV000075900.2,