Original source

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

Alleles
-/A|MAF: 0.17 (A)
Location

Chromosome 16: between 74760600 and 74760601 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs79559612, rs148998226

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays