Original source

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

Alleles
-/A
Location

Chromosome 1: between 149033369 and 149033370 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

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

About this variant

This variant overlaps 13 transcripts and has 1 sample genotype.

Variant displays