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rs63751608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751608(C;C)
Make rs63751608(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042321
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751608
ebirs63751608
HLIrs63751608
Exacrs63751608
Varsomers63751608
Maprs63751608
PheGenIrs63751608
hapmaprs63751608
1000 genomesrs63751608
hgdprs63751608
ensemblrs63751608
gopubmedrs63751608
geneviewrs63751608
scholarrs63751608
googlers63751608
pharmgkbrs63751608
gwascentralrs63751608
openSNPrs63751608
23andMers63751608
23andMe allrs63751608
SNP Nexus

SNPshotrs63751608
SNPdbers63751608
MSV3drs63751608
GWAS Ctlgrs63751608
Max Magnitude0
ClinVar
Risk rs63751608(C;C)
Alt rs63751608(C;C)
Reference rs63751608(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083812T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075320.2,