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rs63751393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751393(C;G)
Make rs63751393(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042283
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751393
ebirs63751393
HLIrs63751393
Exacrs63751393
Varsomers63751393
Maprs63751393
PheGenIrs63751393
hapmaprs63751393
1000 genomesrs63751393
hgdprs63751393
ensemblrs63751393
gopubmedrs63751393
geneviewrs63751393
scholarrs63751393
googlers63751393
pharmgkbrs63751393
gwascentralrs63751393
openSNPrs63751393
23andMers63751393
23andMe allrs63751393
SNP Nexus

SNPshotrs63751393
SNPdbers63751393
MSV3drs63751393
GWAS Ctlgrs63751393
Max Magnitude0
ClinVar
Risk rs63751393(G;G)
Alt rs63751393(G;G)
Reference rs63751393(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083774C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075312.2,