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rs587776622

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776622(A;A)
Make rs587776622(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position75047174
GeneMLH3
is asnp
is mentioned by
dbSNPrs587776622
ebirs587776622
HLIrs587776622
Exacrs587776622
Varsomers587776622
Maprs587776622
PheGenIrs587776622
hapmaprs587776622
1000 genomesrs587776622
hgdprs587776622
ensemblrs587776622
gopubmedrs587776622
geneviewrs587776622
scholarrs587776622
googlers587776622
pharmgkbrs587776622
gwascentralrs587776622
openSNPrs587776622
23andMers587776622
23andMe allrs587776622
SNP Nexus

SNPshotrs587776622
SNPdbers587776622
MSV3drs587776622
GWAS Ctlgrs587776622
Max Magnitude0
ClinVar
Risk rs587776622(A,C;A,C)
Alt rs587776622(A,C;A,C)
Reference rs587776622(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene MLH3
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000014.8:g.75513877C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005896.4,