View genomic variant #0000001296

Chromosome	2
Allele	Unknown
Affects function (reported)	Not classified
Affects function (concluded)	Not classified
DNA change	g.55845109T>C
DB-ID	chr2_000006
Gene	-
dbSNP ID	rs10200159
Risk allele	C
Population	EUROPEAN
Pubmed Reference	Jin et al.(2016)
IGV	NA
1000G	0.145168
gnomAD	0.1389
ExAC	.
GTEx	View in GTEx
Variant remarks	GWAS
Average frequency (large NGS studies)	Retrieve
Owner	IGIB

No variants on transcripts found for this variant!