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rs63751480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751480(C;G)
Make rs63751480(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011852
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751480
ebirs63751480
HLIrs63751480
Exacrs63751480
Varsomers63751480
Maprs63751480
PheGenIrs63751480
hapmaprs63751480
1000 genomesrs63751480
hgdprs63751480
ensemblrs63751480
gopubmedrs63751480
geneviewrs63751480
scholarrs63751480
googlers63751480
pharmgkbrs63751480
gwascentralrs63751480
openSNPrs63751480
23andMers63751480
23andMe allrs63751480
SNP Nexus

SNPshotrs63751480
SNPdbers63751480
MSV3drs63751480
GWAS Ctlgrs63751480
Max Magnitude0
ClinVar
Risk rs63751480(G;G)
Alt rs63751480(G;G)
Reference rs63751480(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053343C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075767.2,