Original source

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

Alleles
-/AA | MAF: 0.38 (-)
Location

Chromosome 10: between 62404127 and 62404128 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2513 individual genotypes.

Variation displays