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rs63751094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751094(A;G)
Make rs63751094(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996624
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751094
ebirs63751094
HLIrs63751094
Exacrs63751094
Varsomers63751094
Maprs63751094
PheGenIrs63751094
hapmaprs63751094
1000 genomesrs63751094
hgdprs63751094
ensemblrs63751094
gopubmedrs63751094
geneviewrs63751094
scholarrs63751094
googlers63751094
pharmgkbrs63751094
gwascentralrs63751094
openSNPrs63751094
23andMers63751094
23andMe allrs63751094
SNP Nexus

SNPshotrs63751094
SNPdbers63751094
MSV3drs63751094
GWAS Ctlgrs63751094
Max Magnitude0
ClinVar
Risk rs63751094(G;G)
Alt rs63751094(G;G)
Reference rs63751094(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038115A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075157.2,