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rs63751439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751439(-;-)
Make rs63751439(-;AAGC)
Make rs63751439(AAGC;AAGC)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017539
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751439
ebirs63751439
HLIrs63751439
Exacrs63751439
Varsomers63751439
Maprs63751439
PheGenIrs63751439
hapmaprs63751439
1000 genomesrs63751439
hgdprs63751439
ensemblrs63751439
gopubmedrs63751439
geneviewrs63751439
scholarrs63751439
googlers63751439
pharmgkbrs63751439
gwascentralrs63751439
openSNPrs63751439
23andMers63751439
23andMe allrs63751439
SNP Nexus

SNPshotrs63751439
SNPdbers63751439
MSV3drs63751439
GWAS Ctlgrs63751439
Max Magnitude0
ClinVar
Risk rs63751439(AAGC;AAGC)
Alt rs63751439(AAGC;AAGC)
Reference rs63751439(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059027_37059030dupAAGC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075879.2,