Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/AT | MAF: 0.42 (-)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386354641, rs386352983

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2514 sample genotypes.

Variant displays