Original source

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

Alleles
-/ATAAG/G | MAF: 0.31 (-)
Location

Chromosome 1: between 236796800 and 236796801 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2504 sample genotypes.

Variant displays