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rs28930073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs28930073(C;C)
Make rs28930073(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007004
GeneMLH1
is asnp
is mentioned by
dbSNPrs28930073
ebirs28930073
HLIrs28930073
Exacrs28930073
Varsomers28930073
Maprs28930073
PheGenIrs28930073
hapmaprs28930073
1000 genomesrs28930073
hgdprs28930073
ensemblrs28930073
gopubmedrs28930073
geneviewrs28930073
scholarrs28930073
googlers28930073
pharmgkbrs28930073
gwascentralrs28930073
openSNPrs28930073
23andMers28930073
23andMe allrs28930073
SNP Nexus

SNPshotrs28930073
SNPdbers28930073
MSV3drs28930073
GWAS Ctlgrs28930073
Merged fromRs121912963
Max Magnitude0
OMIM120436
DescCOLORECTAL CANCER, SPORADIC, SUSCEPTIBILITY TO
Variant0019
Relatedalso

[PMID 19665066] A MLH1 polymorphism that increases cancer risk is associated with better outcome in sporadic colorectal cancer

ClinVar
Risk rs28930073(C;C)
Alt rs28930073(C;C)
Reference rs28930073(G;G)
Significance Other
Disease Colorectal cancer Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MLH1
CLNDBN Colorectal cancer, sporadic, susceptibility to Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37048495G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000018628.2, RCV000075697.5, RCV000115482.6, RCV000200983.2,