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rs63750603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750603(C;C)
Make rs63750603(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37049017
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750603
ebirs63750603
HLIrs63750603
Exacrs63750603
Varsomers63750603
Maprs63750603
PheGenIrs63750603
hapmaprs63750603
1000 genomesrs63750603
hgdprs63750603
ensemblrs63750603
gopubmedrs63750603
geneviewrs63750603
scholarrs63750603
googlers63750603
pharmgkbrs63750603
gwascentralrs63750603
openSNPrs63750603
23andMers63750603
23andMe allrs63750603
SNP Nexus

SNPshotrs63750603
SNPdbers63750603
MSV3drs63750603
GWAS Ctlgrs63750603
Max Magnitude0
ClinVar
Risk rs63750603(A,C;A,C)
Alt rs63750603(A,C;A,C)
Reference rs63750603(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090508G>A; NC_000003.11:g.37090508G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075533.2, RCV000075534.2,