Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G/T|Ancestral: G|Ambiguity code: D|MAF: 0.41 (A)
Location

Chromosome 17:18365454 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2510 sample genotypes.

Variant displays