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rs63750736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750736(G;T)
Make rs63750736(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020314
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750736
ebirs63750736
HLIrs63750736
Exacrs63750736
Varsomers63750736
Maprs63750736
PheGenIrs63750736
hapmaprs63750736
1000 genomesrs63750736
hgdprs63750736
ensemblrs63750736
gopubmedrs63750736
geneviewrs63750736
scholarrs63750736
googlers63750736
pharmgkbrs63750736
gwascentralrs63750736
openSNPrs63750736
23andMers63750736
23andMe allrs63750736
SNP Nexus

SNPshotrs63750736
SNPdbers63750736
MSV3drs63750736
GWAS Ctlgrs63750736
Max Magnitude0
ClinVar
Risk rs63750736(A,T;A,T)
Alt rs63750736(A,T;A,T)
Reference rs63750736(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061805G>A; NC_000003.11:g.37061805G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075926.2, RCV000075927.2,