Original source

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

HGVS names

This variant has 3 HGVS names - Show

About this variant

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

Variant displays