Original source

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


Chromosome 22: between 33285624 and 33285625 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs149082037

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 1 sample genotype.

Variant displays