Original source

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

Alleles
-/A/AA
Location

Chromosome 22: between 42064495 and 42064496 (forward strand)|View in location tab

Co-located variant

dbSNP rs397732719 (-/A)

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays