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rs63751662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751662(G;T)
Make rs63751662(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048609
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751662
ebirs63751662
HLIrs63751662
Exacrs63751662
Varsomers63751662
Maprs63751662
PheGenIrs63751662
hapmaprs63751662
1000 genomesrs63751662
hgdprs63751662
ensemblrs63751662
gopubmedrs63751662
geneviewrs63751662
scholarrs63751662
googlers63751662
pharmgkbrs63751662
gwascentralrs63751662
openSNPrs63751662
23andMers63751662
23andMe allrs63751662
SNP Nexus

SNPshotrs63751662
SNPdbers63751662
MSV3drs63751662
GWAS Ctlgrs63751662
Max Magnitude0
ClinVar
Risk rs63751662(A,T;A,T)
Alt rs63751662(A,T;A,T)
Reference rs63751662(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090100G>A; NC_000003.11:g.37090100G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075461.2, RCV000075462.2,