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
|
No variants on transcripts found for this variant! |
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