Original source

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

Alleles
-/ATAAG/G|MAF: 0.04 (G)
Location

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2504 sample genotypes.

Variant displays