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rs63751460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751460(C;T)
Make rs63751460(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042284
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751460
ebirs63751460
HLIrs63751460
Exacrs63751460
Varsomers63751460
Maprs63751460
PheGenIrs63751460
hapmaprs63751460
1000 genomesrs63751460
hgdprs63751460
ensemblrs63751460
gopubmedrs63751460
geneviewrs63751460
scholarrs63751460
googlers63751460
pharmgkbrs63751460
gwascentralrs63751460
openSNPrs63751460
23andMers63751460
23andMe allrs63751460
SNP Nexus

SNPshotrs63751460
SNPdbers63751460
MSV3drs63751460
GWAS Ctlgrs63751460
Max Magnitude0
ClinVar
Risk rs63751460(T;T)
Alt rs63751460(T;T)
Reference rs63751460(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083775C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075313.2,