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rs63750533

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750533(-;-)
Make rs63750533(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020419
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750533
ebirs63750533
HLIrs63750533
Exacrs63750533
Varsomers63750533
Maprs63750533
PheGenIrs63750533
hapmaprs63750533
1000 genomesrs63750533
hgdprs63750533
ensemblrs63750533
gopubmedrs63750533
geneviewrs63750533
scholarrs63750533
googlers63750533
pharmgkbrs63750533
gwascentralrs63750533
openSNPrs63750533
23andMers63750533
23andMe allrs63750533
SNP Nexus

SNPshotrs63750533
SNPdbers63750533
MSV3drs63750533
GWAS Ctlgrs63750533
Max Magnitude0
ClinVar
Risk rs63750533(;)
Alt rs63750533(;)
Reference rs63750533(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061910delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075956.2,