Original source

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

-/AT | MAF: 0.50 (-)

Chromosome 10: between 48405106 and 48405107 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2510 individual genotypes.

Variation displays