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rs63750212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750212(-;-)
Make rs63750212(-;T)
Make rs63750212(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017571
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750212
ebirs63750212
HLIrs63750212
Exacrs63750212
Varsomers63750212
Maprs63750212
PheGenIrs63750212
hapmaprs63750212
1000 genomesrs63750212
hgdprs63750212
ensemblrs63750212
gopubmedrs63750212
geneviewrs63750212
scholarrs63750212
googlers63750212
pharmgkbrs63750212
gwascentralrs63750212
openSNPrs63750212
23andMers63750212
23andMe allrs63750212
SNP Nexus

SNPshotrs63750212
SNPdbers63750212
MSV3drs63750212
GWAS Ctlgrs63750212
Max Magnitude0
ClinVar
Risk rs63750212(T;T)
Alt rs63750212(T;T)
Reference rs63750212(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059062_37059063insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075888.2,