Original source

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

Alleles
-/A | MAF: 0.43 (T)
Location

Chromosome 1: between 149033370 and 149033371 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts.

Variant displays