Original source

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

-/GTAAG | MAF: 0.02 (GTAAG)

Chromosome 1: between 183555253 and 183555254 (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 12 transcripts and has 2550 sample genotypes.

Variant displays