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rs28939071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28939071(A;A)
Make rs28939071(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position75017093
GeneMLH3
is asnp
is mentioned by
dbSNPrs28939071
ebirs28939071
HLIrs28939071
Exacrs28939071
Varsomers28939071
Maprs28939071
PheGenIrs28939071
hapmaprs28939071
1000 genomesrs28939071
hgdprs28939071
ensemblrs28939071
gopubmedrs28939071
geneviewrs28939071
scholarrs28939071
googlers28939071
pharmgkbrs28939071
gwascentralrs28939071
openSNPrs28939071
23andMers28939071
23andMe allrs28939071
SNP Nexus

SNPshotrs28939071
SNPdbers28939071
MSV3drs28939071
GWAS Ctlgrs28939071
Max Magnitude0
OMIM604395
DescCOLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7
Variant0005
Relatedalso
ClinVar
Risk rs28939071(A;A)
Alt rs28939071(A;A)
Reference rs28939071(G;G)
Significance Non-pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 7 MLH3-Related Lynch Syndrome
Variation info
Gene MLH3
CLNDBN Hereditary nonpolyposis colorectal cancer type 7 MLH3-Related Lynch Syndrome
Reversed 1
HGVS NC_000014.8:g.75483796C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005902.2, RCV000232067.1,