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

rs63750380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750380(-;-)
Make rs63750380(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012071
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750380
ebirs63750380
HLIrs63750380
Exacrs63750380
Varsomers63750380
Maprs63750380
PheGenIrs63750380
hapmaprs63750380
1000 genomesrs63750380
hgdprs63750380
ensemblrs63750380
gopubmedrs63750380
geneviewrs63750380
scholarrs63750380
googlers63750380
pharmgkbrs63750380
gwascentralrs63750380
openSNPrs63750380
23andMers63750380
23andMe allrs63750380
SNP Nexus

SNPshotrs63750380
SNPdbers63750380
MSV3drs63750380
GWAS Ctlgrs63750380
Max Magnitude0
ClinVar
Risk rs63750380(;)
Alt rs63750380(;)
Reference rs63750380(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053562delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075794.2,