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rs63750028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750028(-;-)
Make rs63750028(-;A)
Make rs63750028(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996658
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750028
ebirs63750028
HLIrs63750028
Exacrs63750028
Varsomers63750028
Maprs63750028
PheGenIrs63750028
hapmaprs63750028
1000 genomesrs63750028
hgdprs63750028
ensemblrs63750028
gopubmedrs63750028
geneviewrs63750028
scholarrs63750028
googlers63750028
pharmgkbrs63750028
gwascentralrs63750028
openSNPrs63750028
23andMers63750028
23andMe allrs63750028
SNP Nexus

SNPshotrs63750028
SNPdbers63750028
MSV3drs63750028
GWAS Ctlgrs63750028
Max Magnitude0
ClinVar
Risk rs63750028(A;A)
Alt rs63750028(A;A)
Reference rs63750028(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038149dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075268.2,