View genomic variant #0000001297

Chromosome 2
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change g.112010486T>C
DB-ID chr2_000005
Gene -
dbSNP ID rs4308124
Risk allele C
Population EUROPEAN
Pubmed Reference Jin et al.(2016)
IGV 0.4396
1000G 0.430312
gnomAD 0.4281
ExAC .
GTEx View in GTEx
Variant remarks GWAS
Average frequency (large NGS studies) Retrieve
Owner IGIB




Variant on transcripts

Stop! No variants on transcripts found for this variant!