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rs63751606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751606(C;T)
Make rs63751606(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004472
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751606
ebirs63751606
HLIrs63751606
Exacrs63751606
Varsomers63751606
Maprs63751606
PheGenIrs63751606
hapmaprs63751606
1000 genomesrs63751606
hgdprs63751606
ensemblrs63751606
gopubmedrs63751606
geneviewrs63751606
scholarrs63751606
googlers63751606
pharmgkbrs63751606
gwascentralrs63751606
openSNPrs63751606
23andMers63751606
23andMe allrs63751606
SNP Nexus

SNPshotrs63751606
SNPdbers63751606
MSV3drs63751606
GWAS Ctlgrs63751606
Max Magnitude0
ClinVar
Risk rs63751606(G,T;G,T)
Alt rs63751606(G,T;G,T)
Reference rs63751606(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045963C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075674.2,