Original source

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

Alleles
-/AT | MAF: 0.06 (AT)
Location

Chromosome 1: between 77944321 and 77944322 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2505 sample genotypes.

Variant displays