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

rs63750824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750824(-;-)
Make rs63750824(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040249
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750824
ebirs63750824
HLIrs63750824
Exacrs63750824
Varsomers63750824
Maprs63750824
PheGenIrs63750824
hapmaprs63750824
1000 genomesrs63750824
hgdprs63750824
ensemblrs63750824
gopubmedrs63750824
geneviewrs63750824
scholarrs63750824
googlers63750824
pharmgkbrs63750824
gwascentralrs63750824
openSNPrs63750824
23andMers63750824
23andMe allrs63750824
SNP Nexus

SNPshotrs63750824
SNPdbers63750824
MSV3drs63750824
GWAS Ctlgrs63750824
Max Magnitude0
ClinVar
Risk rs63750824(;)
Alt rs63750824(;)
Reference rs63750824(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081740delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075282.2,