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rs63749916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs63749916(-;-)
Make rs63749916(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028894
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749916
ebirs63749916
HLIrs63749916
Exacrs63749916
Varsomers63749916
Maprs63749916
PheGenIrs63749916
hapmaprs63749916
1000 genomesrs63749916
hgdprs63749916
ensemblrs63749916
gopubmedrs63749916
geneviewrs63749916
scholarrs63749916
googlers63749916
pharmgkbrs63749916
gwascentralrs63749916
openSNPrs63749916
23andMers63749916
23andMe allrs63749916
SNP Nexus

SNPshotrs63749916
SNPdbers63749916
MSV3drs63749916
GWAS Ctlgrs63749916
Max Magnitude0
ClinVar
Risk rs63749916(TT,TTA;TT,TTA)
Alt rs63749916(TT,TTA;TT,TTA)
Reference rs63749916(T;T)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene MLH1
CLNDBN not provided Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070385_37070386insTA; NC_000003.11:g.37070385dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000216066.1, RCV000075233.2,