Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 11:17386218 (forward strand) | View in location tab

Most severe consequence

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts.

Variation displays