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rs63751153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751153(C;T)
Make rs63751153(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025823
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751153
ebirs63751153
HLIrs63751153
Exacrs63751153
Varsomers63751153
Maprs63751153
PheGenIrs63751153
hapmaprs63751153
1000 genomesrs63751153
hgdprs63751153
ensemblrs63751153
gopubmedrs63751153
geneviewrs63751153
scholarrs63751153
googlers63751153
pharmgkbrs63751153
gwascentralrs63751153
openSNPrs63751153
23andMers63751153
23andMe allrs63751153
SNP Nexus

SNPshotrs63751153
SNPdbers63751153
MSV3drs63751153
GWAS Ctlgrs63751153
Max Magnitude0
ClinVar
Risk rs63751153(T;T)
Alt rs63751153(T;T)
Reference rs63751153(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067314C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075156.2,