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rs63750693

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750693(A;A)
Make rs63750693(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047652
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750693
ebirs63750693
HLIrs63750693
Exacrs63750693
Varsomers63750693
Maprs63750693
PheGenIrs63750693
hapmaprs63750693
1000 genomesrs63750693
hgdprs63750693
ensemblrs63750693
gopubmedrs63750693
geneviewrs63750693
scholarrs63750693
googlers63750693
pharmgkbrs63750693
gwascentralrs63750693
openSNPrs63750693
23andMers63750693
23andMe allrs63750693
SNP Nexus

SNPshotrs63750693
SNPdbers63750693
MSV3drs63750693
GWAS Ctlgrs63750693
Max Magnitude0
ClinVar
Risk rs63750693(A,C;A,C)
Alt rs63750693(A,C;A,C)
Reference rs63750693(T;T)
Significance Pathogenic
Disease Lynch syndrome II Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome II Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089143T>A; NC_000003.11:g.37089143T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000022505.27, RCV000075389.2, RCV000075390.3,