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rs63750853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750853(-;-)
Make rs63750853(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020436
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750853
ebirs63750853
HLIrs63750853
Exacrs63750853
Varsomers63750853
Maprs63750853
PheGenIrs63750853
hapmaprs63750853
1000 genomesrs63750853
hgdprs63750853
ensemblrs63750853
gopubmedrs63750853
geneviewrs63750853
scholarrs63750853
googlers63750853
pharmgkbrs63750853
gwascentralrs63750853
openSNPrs63750853
23andMers63750853
23andMe allrs63750853
SNP Nexus

SNPshotrs63750853
SNPdbers63750853
MSV3drs63750853
GWAS Ctlgrs63750853
Max Magnitude0
ClinVar
Risk rs63750853(;)
Alt rs63750853(;)
Reference rs63750853(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061927delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075072.2,