Original source

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

Alleles
-/TTTG
Location

Chromosome 5: between 132299599 and 132299600 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs148686460

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays