Original source

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

-/AT|MAF: 0.42 (-)

Chromosome 1: between 225409161 and 225409162 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386354641, rs386352983

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2514 sample genotypes.

Variant displays