Original source

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

-/TTC | MAF: 0.10 (TTC)

Chromosome 2: between 9489169 and 9489170 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs147309883

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2504 sample genotypes.

Variant displays