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

rs63750507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750507(G;G)
Make rs63750507(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004414
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750507
ebirs63750507
HLIrs63750507
Exacrs63750507
Varsomers63750507
Maprs63750507
PheGenIrs63750507
hapmaprs63750507
1000 genomesrs63750507
hgdprs63750507
ensemblrs63750507
gopubmedrs63750507
geneviewrs63750507
scholarrs63750507
googlers63750507
pharmgkbrs63750507
gwascentralrs63750507
openSNPrs63750507
23andMers63750507
23andMe allrs63750507
SNP Nexus

SNPshotrs63750507
SNPdbers63750507
MSV3drs63750507
GWAS Ctlgrs63750507
Max Magnitude0
ClinVar
Risk rs63750507(G;G)
Alt rs63750507(G;G)
Reference rs63750507(T;T)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37045905T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075654.2, RCV000160517.1,