Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751468(-;-)
Make rs63751468(-;A)
Make rs63751468(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028788
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751468
ebirs63751468
HLIrs63751468
Exacrs63751468
Varsomers63751468
Maprs63751468
PheGenIrs63751468
hapmaprs63751468
1000 genomesrs63751468
hgdprs63751468
ensemblrs63751468
gopubmedrs63751468
geneviewrs63751468
scholarrs63751468
googlers63751468
pharmgkbrs63751468
gwascentralrs63751468
openSNPrs63751468
23andMers63751468
23andMe allrs63751468
SNP Nexus

SNPshotrs63751468
SNPdbers63751468
MSV3drs63751468
GWAS Ctlgrs63751468
Max Magnitude0
ClinVar
Risk rs63751468(A;A)
Alt rs63751468(A;A)
Reference rs63751468(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070279dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075205.2,