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rs63750819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750819(-;-)
Make rs63750819(-;G)
Make rs63750819(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014499
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750819
ebirs63750819
HLIrs63750819
Exacrs63750819
Varsomers63750819
Maprs63750819
PheGenIrs63750819
hapmaprs63750819
1000 genomesrs63750819
hgdprs63750819
ensemblrs63750819
gopubmedrs63750819
geneviewrs63750819
scholarrs63750819
googlers63750819
pharmgkbrs63750819
gwascentralrs63750819
openSNPrs63750819
23andMers63750819
23andMe allrs63750819
SNP Nexus

SNPshotrs63750819
SNPdbers63750819
MSV3drs63750819
GWAS Ctlgrs63750819
Max Magnitude0
ClinVar
Risk rs63750819(G;G)
Alt rs63750819(G;G)
Reference rs63750819(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055990dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075836.2,