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rs63750385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750385(-;-)
Make rs63750385(-;A)
Make rs63750385(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012087
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750385
ebirs63750385
HLIrs63750385
Exacrs63750385
Varsomers63750385
Maprs63750385
PheGenIrs63750385
hapmaprs63750385
1000 genomesrs63750385
hgdprs63750385
ensemblrs63750385
gopubmedrs63750385
geneviewrs63750385
scholarrs63750385
googlers63750385
pharmgkbrs63750385
gwascentralrs63750385
openSNPrs63750385
23andMers63750385
23andMe allrs63750385
SNP Nexus

SNPshotrs63750385
SNPdbers63750385
MSV3drs63750385
GWAS Ctlgrs63750385
Max Magnitude0
ClinVar
Risk rs63750385(A;A)
Alt rs63750385(A;A)
Reference rs63750385(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053578dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075798.2,