Original source

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

AA/- | MAF: 0.35 (AA)

Chromosome 19:16486620-16486621 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs373470899

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

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays