Original source

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

Alleles
ATTC/-
Location

Chromosome 1:12170177-12170180 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs56828712

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts.

Variant displays