Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 16:74744451 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60053618

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays