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rs63750748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750748(-;-)
Make rs63750748(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025908
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750748
ebirs63750748
HLIrs63750748
Exacrs63750748
Varsomers63750748
Maprs63750748
PheGenIrs63750748
hapmaprs63750748
1000 genomesrs63750748
hgdprs63750748
ensemblrs63750748
gopubmedrs63750748
geneviewrs63750748
scholarrs63750748
googlers63750748
pharmgkbrs63750748
gwascentralrs63750748
openSNPrs63750748
23andMers63750748
23andMe allrs63750748
SNP Nexus

SNPshotrs63750748
SNPdbers63750748
MSV3drs63750748
GWAS Ctlgrs63750748
Max Magnitude0
ClinVar
Risk rs63750748(;)
Alt rs63750748(;)
Reference rs63750748(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067399delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075168.2,