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rs63750193

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750193(C;C)
Make rs63750193(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040276
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750193
ebirs63750193
HLIrs63750193
Exacrs63750193
Varsomers63750193
Maprs63750193
PheGenIrs63750193
hapmaprs63750193
1000 genomesrs63750193
hgdprs63750193
ensemblrs63750193
gopubmedrs63750193
geneviewrs63750193
scholarrs63750193
googlers63750193
pharmgkbrs63750193
gwascentralrs63750193
openSNPrs63750193
23andMers63750193
23andMe allrs63750193
SNP Nexus

SNPshotrs63750193
SNPdbers63750193
MSV3drs63750193
GWAS Ctlgrs63750193
Max Magnitude0
ClinVar
Risk rs63750193(C;C)
Alt rs63750193(C;C)
Reference rs63750193(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081767T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075292.2,