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rs63750482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750482(-;-)
Make rs63750482(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028794
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750482
ebirs63750482
HLIrs63750482
Exacrs63750482
Varsomers63750482
Maprs63750482
PheGenIrs63750482
hapmaprs63750482
1000 genomesrs63750482
hgdprs63750482
ensemblrs63750482
gopubmedrs63750482
geneviewrs63750482
scholarrs63750482
googlers63750482
pharmgkbrs63750482
gwascentralrs63750482
openSNPrs63750482
23andMers63750482
23andMe allrs63750482
SNP Nexus

SNPshotrs63750482
SNPdbers63750482
MSV3drs63750482
GWAS Ctlgrs63750482
Max Magnitude0
ClinVar
Risk rs63750482(;)
Alt rs63750482(;)
Reference rs63750482(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070285delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075210.2,