Original source

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

Alleles
GA/- | MAF: 0.01 (-)
Location

Chromosome 19:42086701-42086702 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2504 individual genotypes.

Variation displays