Original source

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

-/ACTG/GTCT/TCTG | MAF: 0.23 (-)

Chromosome 1: between 236815692 and 236815693 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs140643649

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays