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rs63750740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750740(-;-)
Make rs63750740(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048923
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750740
ebirs63750740
HLIrs63750740
Exacrs63750740
Varsomers63750740
Maprs63750740
PheGenIrs63750740
hapmaprs63750740
1000 genomesrs63750740
hgdprs63750740
ensemblrs63750740
gopubmedrs63750740
geneviewrs63750740
scholarrs63750740
googlers63750740
pharmgkbrs63750740
gwascentralrs63750740
openSNPrs63750740
23andMers63750740
23andMe allrs63750740
SNP Nexus

SNPshotrs63750740
SNPdbers63750740
MSV3drs63750740
GWAS Ctlgrs63750740
Max Magnitude0
ClinVar
Risk rs63750740(;)
Alt rs63750740(;)
Reference rs63750740(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090414delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075481.2,