Original source

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

Alleles
-/GTTT/GTTTGTTTGTTTGTTT
Location

Chromosome 1: between 26714429 and 26714430 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs397979729

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2 sample genotypes.

Variant displays