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rs63750948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750948(G;G)
Make rs63750948(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014493
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750948
ebirs63750948
HLIrs63750948
Exacrs63750948
Varsomers63750948
Maprs63750948
PheGenIrs63750948
hapmaprs63750948
1000 genomesrs63750948
hgdprs63750948
ensemblrs63750948
gopubmedrs63750948
geneviewrs63750948
scholarrs63750948
googlers63750948
pharmgkbrs63750948
gwascentralrs63750948
openSNPrs63750948
23andMers63750948
23andMe allrs63750948
SNP Nexus

SNPshotrs63750948
SNPdbers63750948
MSV3drs63750948
GWAS Ctlgrs63750948
Max Magnitude0
ClinVar
Risk rs63750948(C,G;C,G)
Alt rs63750948(C,G;C,G)
Reference rs63750948(T;T)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37055984T>C; NC_000003.11:g.37055984T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075833.2, RCV000114847.1,