Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: < 0.01 (T)
Location

Chromosome 9:2013521 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.2013521A>T

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays