Original source

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

Alleles
-/AGAC|MAF: 0.22 (-)
Location

Chromosome 4: between 174515617 and 174515618 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs139940528

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays