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rs63750855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750855(-;-)
Make rs63750855(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028863
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750855
ebirs63750855
HLIrs63750855
Exacrs63750855
Varsomers63750855
Maprs63750855
PheGenIrs63750855
hapmaprs63750855
1000 genomesrs63750855
hgdprs63750855
ensemblrs63750855
gopubmedrs63750855
geneviewrs63750855
scholarrs63750855
googlers63750855
pharmgkbrs63750855
gwascentralrs63750855
openSNPrs63750855
23andMers63750855
23andMe allrs63750855
SNP Nexus

SNPshotrs63750855
SNPdbers63750855
MSV3drs63750855
GWAS Ctlgrs63750855
Max Magnitude0
ClinVar
Risk rs63750855(;)
Alt rs63750855(;)
Reference rs63750855(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070354delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075226.2,