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rs63750375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs63750375(-;-)
Make rs63750375(-;CA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047565
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750375
ebirs63750375
HLIrs63750375
Exacrs63750375
Varsomers63750375
Maprs63750375
PheGenIrs63750375
hapmaprs63750375
1000 genomesrs63750375
hgdprs63750375
ensemblrs63750375
gopubmedrs63750375
geneviewrs63750375
scholarrs63750375
googlers63750375
pharmgkbrs63750375
gwascentralrs63750375
openSNPrs63750375
23andMers63750375
23andMe allrs63750375
SNP Nexus

SNPshotrs63750375
SNPdbers63750375
MSV3drs63750375
GWAS Ctlgrs63750375
Max Magnitude0
ClinVar
Risk rs63750375(;)
Alt rs63750375(;)
Reference rs63750375(CA;CA)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37089056_37089057delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075363.2, RCV000202156.1,