Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/ATT | MAF: 0.48 (ATT)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs149223350

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2512 sample genotypes.

Variant displays