Original source

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

TG/- | MAF: 0.27 (-)

Chromosome 8:42482737-42482738 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs143885739

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2506 sample genotypes.

Variant displays