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rs63751653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63751653(-;-)
Make rs63751653(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011862
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751653
ebirs63751653
HLIrs63751653
Exacrs63751653
Varsomers63751653
Maprs63751653
PheGenIrs63751653
hapmaprs63751653
1000 genomesrs63751653
hgdprs63751653
ensemblrs63751653
gopubmedrs63751653
geneviewrs63751653
scholarrs63751653
googlers63751653
pharmgkbrs63751653
gwascentralrs63751653
openSNPrs63751653
23andMers63751653
23andMe allrs63751653
SNP Nexus

SNPshotrs63751653
SNPdbers63751653
MSV3drs63751653
GWAS Ctlgrs63751653
Max Magnitude0
ClinVar
Risk rs63751653(;)
Alt rs63751653(;)
Reference rs63751653(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053353delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075776.2,