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rs63750300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750300(A;A)
Make rs63750300(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040267
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750300
ebirs63750300
HLIrs63750300
Exacrs63750300
Varsomers63750300
Maprs63750300
PheGenIrs63750300
hapmaprs63750300
1000 genomesrs63750300
hgdprs63750300
ensemblrs63750300
gopubmedrs63750300
geneviewrs63750300
scholarrs63750300
googlers63750300
pharmgkbrs63750300
gwascentralrs63750300
openSNPrs63750300
23andMers63750300
23andMe allrs63750300
SNP Nexus

SNPshotrs63750300
SNPdbers63750300
MSV3drs63750300
GWAS Ctlgrs63750300
Max Magnitude0
ClinVar
Risk rs63750300(A;A)
Alt rs63750300(A;A)
Reference rs63750300(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081758T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075288.2,