Rs121908439

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Orientationminus
is asnp
is mentioned by
dbSNPrs121908439
PheGenIrs121908439
nextbiors121908439
hapmaprs121908439
1000 genomesrs121908439
hgdprs121908439
ensemblrs121908439
gopubmedrs121908439
geneviewrs121908439
scholarrs121908439
googlers121908439
pharmgkbrs121908439
gwascentralrs121908439
openSNPrs121908439
23andMers121908439
23andMe allrs121908439
SNP Nexus

SNPshotrs121908439
SNPdbers121908439
MSV3drs121908439
GeneMLH3
Chromosome14
Orientationminus
Position75032069
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908439(C;C)
Make rs121908439(C;T)
OMIM604395
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908439(C;C)
Alt rs121908439(C;C)
Reference rs121908439(T;T)
Significance 5
Disease Hereditary nonpolyposis colorectal cancer type 7
ClinVar info
Gene MLH3
CLNDBN Hereditary nonpolyposis colorectal cancer type 7
Reversed 1
CLNHGVS NC_000014.8:g.75498772A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005905.1