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

rs63750115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750115(-;-)
Make rs63750115(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048591
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750115
ebirs63750115
HLIrs63750115
Exacrs63750115
Varsomers63750115
Maprs63750115
PheGenIrs63750115
hapmaprs63750115
1000 genomesrs63750115
hgdprs63750115
ensemblrs63750115
gopubmedrs63750115
geneviewrs63750115
scholarrs63750115
googlers63750115
pharmgkbrs63750115
gwascentralrs63750115
openSNPrs63750115
23andMers63750115
23andMe allrs63750115
SNP Nexus

SNPshotrs63750115
SNPdbers63750115
MSV3drs63750115
GWAS Ctlgrs63750115
Max Magnitude0
ClinVar
Risk rs63750115(;)
Alt rs63750115(;)
Reference rs63750115(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090082delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075443.2,