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rs63751421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751421(C;T)
Make rs63751421(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001003
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751421
ebirs63751421
HLIrs63751421
Exacrs63751421
Varsomers63751421
Maprs63751421
PheGenIrs63751421
hapmaprs63751421
1000 genomesrs63751421
hgdprs63751421
ensemblrs63751421
gopubmedrs63751421
geneviewrs63751421
scholarrs63751421
googlers63751421
pharmgkbrs63751421
gwascentralrs63751421
openSNPrs63751421
23andMers63751421
23andMe allrs63751421
SNP Nexus

SNPshotrs63751421
SNPdbers63751421
MSV3drs63751421
GWAS Ctlgrs63751421
Max Magnitude0
ClinVar
Risk rs63751421(T;T)
Alt rs63751421(T;T)
Reference rs63751421(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042494C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075607.2,