Original source

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

Alleles
CA/-
Location

Chromosome 5:159328344-159328345 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs376537579, rs145917395

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays