Have questions? Visit https://www.reddit.com/r/SNPedia

rs63749863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749863(-;-)
Make rs63749863(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047545
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749863
ebirs63749863
HLIrs63749863
Exacrs63749863
Varsomers63749863
Maprs63749863
PheGenIrs63749863
hapmaprs63749863
1000 genomesrs63749863
hgdprs63749863
ensemblrs63749863
gopubmedrs63749863
geneviewrs63749863
scholarrs63749863
googlers63749863
pharmgkbrs63749863
gwascentralrs63749863
openSNPrs63749863
23andMers63749863
23andMe allrs63749863
SNP Nexus

SNPshotrs63749863
SNPdbers63749863
MSV3drs63749863
GWAS Ctlgrs63749863
Max Magnitude0
ClinVar
Risk rs63749863(;)
Alt rs63749863(;)
Reference rs63749863(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089036delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075354.2,