View genomic variant #0000001066

Chromosome 6
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change g.29943067G>A
DB-ID HCG9_000001
Gene HCG9
dbSNP ID rs6904029
Risk allele A
Population EUROPEAN
Pubmed Reference Jin et al.(2010)
IGV 0.1667
1000G 0.25599
gnomAD 0.2774
ExAC 0.3413
GTEx View in GTEx
Variant remarks GWAS
Average frequency (large NGS studies) 0.24781 View details
Owner IGIB




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HCG9 NR_028032.1 ./. - n.176G>A - -