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rs121912959

From SNPedia

Merged intors63750206
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912959(G;T)
Make rs121912959(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996701
GeneMLH1
is asnp
is mentioned by
dbSNPrs121912959
ebirs121912959
HLIrs121912959
Exacrs121912959
Varsomers121912959
Maprs121912959
PheGenIrs121912959
hapmaprs121912959
1000 genomesrs121912959
hgdprs121912959
ensemblrs121912959
gopubmedrs121912959
geneviewrs121912959
scholarrs121912959
googlers121912959
pharmgkbrs121912959
gwascentralrs121912959
openSNPrs121912959
23andMers121912959
23andMe allrs121912959
SNP Nexus

SNPshotrs121912959
SNPdbers121912959
MSV3drs121912959
GWAS Ctlgrs121912959
StatusMerged into rs63750206
Max Magnitude0
OMIM120436
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121912959(T;T)
Alt rs121912959(T;T)
Reference rs121912959(G;G)
Significance Pathogenic
Disease Lynch syndrome II Turcot syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome II Turcot syndrome
Reversed 0
HGVS NC_000003.11:g.37038192G>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000038901.1, SCV000038902.1,