Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 19:1220322 (forward strand) | View in location tab

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

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2506 individual genotypes and is mentioned in 1 citation.

Variation displays