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rs63750769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs63750769(-;-)
Make rs63750769(-;TG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048990
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750769
ebirs63750769
HLIrs63750769
Exacrs63750769
Varsomers63750769
Maprs63750769
PheGenIrs63750769
hapmaprs63750769
1000 genomesrs63750769
hgdprs63750769
ensemblrs63750769
gopubmedrs63750769
geneviewrs63750769
scholarrs63750769
googlers63750769
pharmgkbrs63750769
gwascentralrs63750769
openSNPrs63750769
23andMers63750769
23andMe allrs63750769
SNP Nexus

SNPshotrs63750769
SNPdbers63750769
MSV3drs63750769
GWAS Ctlgrs63750769
Max Magnitude0
ClinVar
Risk rs63750769(;)
Alt rs63750769(;)
Reference rs63750769(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090481_37090482delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075510.2,