Original source

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

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 1 sample genotype.

Variant displays