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rs63750713

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750713(-;-)
Make rs63750713(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025996
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750713
ebirs63750713
HLIrs63750713
Exacrs63750713
Varsomers63750713
Maprs63750713
PheGenIrs63750713
hapmaprs63750713
1000 genomesrs63750713
hgdprs63750713
ensemblrs63750713
gopubmedrs63750713
geneviewrs63750713
scholarrs63750713
googlers63750713
pharmgkbrs63750713
gwascentralrs63750713
openSNPrs63750713
23andMers63750713
23andMe allrs63750713
SNP Nexus

SNPshotrs63750713
SNPdbers63750713
MSV3drs63750713
GWAS Ctlgrs63750713
Max Magnitude0
ClinVar
Risk rs63750713(;)
Alt rs63750713(;)
Reference rs63750713(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067487delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075187.2,