Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 16:30751910 (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 rs57330689

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2511 individual genotypes.

Variation displays