Original source

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

Alleles
-/A
Location

Chromosome 4: between 89794716 and 89794717 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs72624321, rs72614928

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts.

Variant displays