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rs63750677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750677(-;-)
Make rs63750677(-;C)
Make rs63750677(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020436
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750677
ebirs63750677
HLIrs63750677
Exacrs63750677
Varsomers63750677
Maprs63750677
PheGenIrs63750677
hapmaprs63750677
1000 genomesrs63750677
hgdprs63750677
ensemblrs63750677
gopubmedrs63750677
geneviewrs63750677
scholarrs63750677
googlers63750677
pharmgkbrs63750677
gwascentralrs63750677
openSNPrs63750677
23andMers63750677
23andMe allrs63750677
SNP Nexus

SNPshotrs63750677
SNPdbers63750677
MSV3drs63750677
GWAS Ctlgrs63750677
Max Magnitude0
ClinVar
Risk rs63750677(C;C)
Alt rs63750677(C;C)
Reference rs63750677(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061927dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075073.3,