Original source

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

T/- | Ancestral: T

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

Most severe consequence
Intron variant
Evidence status


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