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rs63749818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749818(A;A)
Make rs63749818(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007002
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749818
ebirs63749818
HLIrs63749818
Exacrs63749818
Varsomers63749818
Maprs63749818
PheGenIrs63749818
hapmaprs63749818
1000 genomesrs63749818
hgdprs63749818
ensemblrs63749818
gopubmedrs63749818
geneviewrs63749818
scholarrs63749818
googlers63749818
pharmgkbrs63749818
gwascentralrs63749818
openSNPrs63749818
23andMers63749818
23andMe allrs63749818
SNP Nexus

SNPshotrs63749818
SNPdbers63749818
MSV3drs63749818
GWAS Ctlgrs63749818
Max Magnitude0
ClinVar
Risk rs63749818(A,G;A,G)
Alt rs63749818(A,G;A,G)
Reference rs63749818(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37048493C>A; NC_000003.11:g.37048493C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075696.2, RCV000220277.1,