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rs63750211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750211(A;G)
Make rs63750211(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008904
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750211
ebirs63750211
HLIrs63750211
Exacrs63750211
Varsomers63750211
Maprs63750211
PheGenIrs63750211
hapmaprs63750211
1000 genomesrs63750211
hgdprs63750211
ensemblrs63750211
gopubmedrs63750211
geneviewrs63750211
scholarrs63750211
googlers63750211
pharmgkbrs63750211
gwascentralrs63750211
openSNPrs63750211
23andMers63750211
23andMe allrs63750211
SNP Nexus

SNPshotrs63750211
SNPdbers63750211
MSV3drs63750211
GWAS Ctlgrs63750211
Max Magnitude0
ClinVar
Risk rs63750211(G;G)
Alt rs63750211(G;G)
Reference rs63750211(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050395A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075747.3,