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rs63750639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750639(A;A)
Make rs63750639(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048912
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750639
ebirs63750639
HLIrs63750639
Exacrs63750639
Varsomers63750639
Maprs63750639
PheGenIrs63750639
hapmaprs63750639
1000 genomesrs63750639
hgdprs63750639
ensemblrs63750639
gopubmedrs63750639
geneviewrs63750639
scholarrs63750639
googlers63750639
pharmgkbrs63750639
gwascentralrs63750639
openSNPrs63750639
23andMers63750639
23andMe allrs63750639
SNP Nexus

SNPshotrs63750639
SNPdbers63750639
MSV3drs63750639
GWAS Ctlgrs63750639
Max Magnitude0
ClinVar
Risk rs63750639(A;A)
Alt rs63750639(A;A)
Reference rs63750639(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090403G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075473.2,