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rs63749868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATAG;ATAG) 0 common in clinvar
(TAGA;TAGA) 0 common in clinvar
Make rs63749868(-;-)
Make rs63749868(-;ATAG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047559
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749868
ebirs63749868
HLIrs63749868
Exacrs63749868
Varsomers63749868
Maprs63749868
PheGenIrs63749868
hapmaprs63749868
1000 genomesrs63749868
hgdprs63749868
ensemblrs63749868
gopubmedrs63749868
geneviewrs63749868
scholarrs63749868
googlers63749868
pharmgkbrs63749868
gwascentralrs63749868
openSNPrs63749868
23andMers63749868
23andMe allrs63749868
SNP Nexus

SNPshotrs63749868
SNPdbers63749868
MSV3drs63749868
GWAS Ctlgrs63749868
Max Magnitude0
ClinVar
Risk rs63749868(;)
Alt rs63749868(;)
Reference rs63749868(TAGA;TAGA)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37089050_37089053delATAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075362.2, RCV000202011.1,