Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 17:17236983 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 2510 sample genotypes and is mentioned in 1 citation.

Variant displays