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rs6594681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6594681(C;T)
Make rs6594681(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position113104244
GeneMCC
is asnp
is mentioned by
dbSNPrs6594681
ebirs6594681
HLIrs6594681
Exacrs6594681
Varsomers6594681
Maprs6594681
PheGenIrs6594681
hapmaprs6594681
1000 genomesrs6594681
hgdprs6594681
ensemblrs6594681
gopubmedrs6594681
geneviewrs6594681
scholarrs6594681
googlers6594681
pharmgkbrs6594681
gwascentralrs6594681
openSNPrs6594681
23andMers6594681
23andMe allrs6594681
SNP Nexus

SNPshotrs6594681
SNPdbers6594681
MSV3drs6594681
GWAS Ctlgrs6594681
GMAF0.002296
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Venter snp
Source plos
Gene MCC
allele C
frequency 1
sift TOLERATED
HuRef 1103654193136
Disease Association Is probably involved in early stages of colorectal neoplasia in both sporadic and familial tumors.



GET Evidence
MCC-K380R
aa_change Lys380Arg
aa_change_short K380R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.992841
summary