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rs63750908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750908(-;-)
Make rs63750908(-;T)
Make rs63750908(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012054
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750908
ebirs63750908
HLIrs63750908
Exacrs63750908
Varsomers63750908
Maprs63750908
PheGenIrs63750908
hapmaprs63750908
1000 genomesrs63750908
hgdprs63750908
ensemblrs63750908
gopubmedrs63750908
geneviewrs63750908
scholarrs63750908
googlers63750908
pharmgkbrs63750908
gwascentralrs63750908
openSNPrs63750908
23andMers63750908
23andMe allrs63750908
SNP Nexus

SNPshotrs63750908
SNPdbers63750908
MSV3drs63750908
GWAS Ctlgrs63750908
Max Magnitude0
ClinVar
Risk rs63750908(T;T)
Alt rs63750908(T;T)
Reference rs63750908(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053545_37053546insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075788.2,