Original source

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

Alleles
-/ATG
Location

Chromosome 2: between 85886175 and 85886176 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs76862052

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad

Variation displays