Original source

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

Alleles
-/T | MAF: 0.45 (-)
Location

Chromosome 19: between 49476584 and 49476585 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

Variation displays