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rs28937870

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0
Make rs28937870(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position75049586
GeneMLH3
is asnp
is mentioned by
dbSNPrs28937870
ebirs28937870
HLIrs28937870
Exacrs28937870
Varsomers28937870
Maprs28937870
PheGenIrs28937870
hapmaprs28937870
1000 genomesrs28937870
hgdprs28937870
ensemblrs28937870
gopubmedrs28937870
geneviewrs28937870
scholarrs28937870
googlers28937870
pharmgkbrs28937870
gwascentralrs28937870
openSNPrs28937870
23andMers28937870
23andMe allrs28937870
SNP Nexus

SNPshotrs28937870
SNPdbers28937870
MSV3drs28937870
GWAS Ctlgrs28937870
Max Magnitude0
OMIM604395
DescCOLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7
Variant0002
Relatedalso


ClinVar
Risk rs28937870(G;G)
Alt rs28937870(G;G)
Reference rs28937870(C;C)
Significance Unknown
Disease Hereditary nonpolyposis colorectal cancer type 7
Variation info
Gene MLH3
CLNDBN Hereditary nonpolyposis colorectal cancer type 7
Reversed 1
HGVS NC_000014.8:g.75516289G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005897.2,