Original source

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

Alleles
-/A
Location

Chromosome 22: between 33324261 and 33324262 (forward strand)|View in location tab

Co-located variant

dbSNP rs71326530 (A/C)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs372619794

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays