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rs63750499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750499(A;A)
Make rs63750499(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050518
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750499
ebirs63750499
HLIrs63750499
Exacrs63750499
Varsomers63750499
Maprs63750499
PheGenIrs63750499
hapmaprs63750499
1000 genomesrs63750499
hgdprs63750499
ensemblrs63750499
gopubmedrs63750499
geneviewrs63750499
scholarrs63750499
googlers63750499
pharmgkbrs63750499
gwascentralrs63750499
openSNPrs63750499
23andMers63750499
23andMe allrs63750499
SNP Nexus

SNPshotrs63750499
SNPdbers63750499
MSV3drs63750499
GWAS Ctlgrs63750499
Max Magnitude0
ClinVar
Risk rs63750499(A,T;A,T)
Alt rs63750499(A,T;A,T)
Reference rs63750499(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092009G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075551.2,