RNF181
Cancer Mutation
SNP
mRNA Expression
DNA & RNA Element
PPI
Disease
PTM
DNA Methylation
Proteomics
GWASdb
GWAS Central
OMIM
Disease associated variation - GWASdb
Chr
Pos
SNP ID(dbSNP 142)
Ref
Alt
Ori SNP ID
P-value
Drug Name
Drug Anno
GWAS Trait
HPO ID
DO ID
AA
Type
Trait or Drug
2
85824251
rs6643
T
C
rs6643
6.58E-04
Glycosylated haemoglobin levels
HPOID:0011902|HPOID:0000077|HPOID:0001626|HPOID:0000819|HPOID:0000479
DOID:1287|DOID:9351|DOID:557|DOID:5679
C
missense
GWASdb_trait
2
85824468
rs2232750
C
T
rs2232750
7.06E-05
Lymphocyte counts
HPOID:0004332|HPOID:0002665
DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287
C
intron
GWASdb_trait
Disease associated variation - GWAS Central
Study Name
Source Marker Accession
Chromosome
Marker Start
Marker Stop
Alleles
Gene Section
P-value
-log(p-value)
GWAS of prostate cancer
rs6643
2
85824251
85824251
exonic
0.879124
0.0559498635864758
Disease associated variation - OMIM
Ensembl_gene_ID
Approved Gene Symbol
MIM Number
ENSG00000168894.9
RNF181
612490