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rs63749959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63749959(-;-)
Make rs63749959(-;A)
Make rs63749959(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008863
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749959
ebirs63749959
HLIrs63749959
Exacrs63749959
Varsomers63749959
Maprs63749959
PheGenIrs63749959
hapmaprs63749959
1000 genomesrs63749959
hgdprs63749959
ensemblrs63749959
gopubmedrs63749959
geneviewrs63749959
scholarrs63749959
googlers63749959
pharmgkbrs63749959
gwascentralrs63749959
openSNPrs63749959
23andMers63749959
23andMe allrs63749959
SNP Nexus

SNPshotrs63749959
SNPdbers63749959
MSV3drs63749959
GWAS Ctlgrs63749959
Max Magnitude0
ClinVar
Risk rs63749959(A;A)
Alt rs63749959(A;A)
Reference rs63749959(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050354dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075739.2,