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rs63750483

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750483(C;T)
Make rs63750483(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025790
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750483
ebirs63750483
HLIrs63750483
Exacrs63750483
Varsomers63750483
Maprs63750483
PheGenIrs63750483
hapmaprs63750483
1000 genomesrs63750483
hgdprs63750483
ensemblrs63750483
gopubmedrs63750483
geneviewrs63750483
scholarrs63750483
googlers63750483
pharmgkbrs63750483
gwascentralrs63750483
openSNPrs63750483
23andMers63750483
23andMe allrs63750483
SNP Nexus

SNPshotrs63750483
SNPdbers63750483
MSV3drs63750483
GWAS Ctlgrs63750483
Max Magnitude0
ClinVar
Risk rs63750483(G,T;G,T)
Alt rs63750483(G,T;G,T)
Reference rs63750483(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067281C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075146.2,