Original source

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

-/ATT|MAF: 0.48 (ATT)

Chromosome 12: between 20832950 and 20832951 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs149223350

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2512 sample genotypes.

Variant displays