Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.13 (A)
Location

Chromosome 19:33300221 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3684 sample genotypes and is mentioned in 4 citations.

Variant displays