Original source

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

Alleles
-/A/AT
Location

Chromosome 1: between 225409163 and 225409164 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs148029475, rs59516424

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 1 sample genotype.

Variant displays