Original source

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

Alleles
ACAAA/-|MAF: 0.24 (-)
Location

Chromosome 16:50752262-50752266 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs151087977

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2508 sample genotypes.

Variant displays