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rs63751087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751087(C;G)
Make rs63751087(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040271
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751087
ebirs63751087
HLIrs63751087
Exacrs63751087
Varsomers63751087
Maprs63751087
PheGenIrs63751087
hapmaprs63751087
1000 genomesrs63751087
hgdprs63751087
ensemblrs63751087
gopubmedrs63751087
geneviewrs63751087
scholarrs63751087
googlers63751087
pharmgkbrs63751087
gwascentralrs63751087
openSNPrs63751087
23andMers63751087
23andMe allrs63751087
SNP Nexus

SNPshotrs63751087
SNPdbers63751087
MSV3drs63751087
GWAS Ctlgrs63751087
Max Magnitude0
ClinVar
Risk rs63751087(G;G)
Alt rs63751087(G;G)
Reference rs63751087(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081762C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075289.2,