Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 16:89770457 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs17226631, rs57207075

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2598 individual genotypes.

Variation displays