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rs63751277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751277(C;T)
Make rs63751277(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040236
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751277
ebirs63751277
HLIrs63751277
Exacrs63751277
Varsomers63751277
Maprs63751277
PheGenIrs63751277
hapmaprs63751277
1000 genomesrs63751277
hgdprs63751277
ensemblrs63751277
gopubmedrs63751277
geneviewrs63751277
scholarrs63751277
googlers63751277
pharmgkbrs63751277
gwascentralrs63751277
openSNPrs63751277
23andMers63751277
23andMe allrs63751277
SNP Nexus

SNPshotrs63751277
SNPdbers63751277
MSV3drs63751277
GWAS Ctlgrs63751277
Max Magnitude0
ClinVar
Risk rs63751277(T;T)
Alt rs63751277(T;T)
Reference rs63751277(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081727C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075275.2,