Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/A/AA
Location

Chromosome 1: between 92183262 and 92183263 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 14 HGVS names - click the plus to show

Variation displays