Original source

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

Alleles
-/GTAA/GTAAG|MAF: 0.02 (GTAAG)
Location

Chromosome 1: between 183555253 and 183555254 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2550 sample genotypes.

Variant displays