Original source

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

AT/- | MAF: 0.12 (-)

Chromosome 19:42355256-42355257 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs146191696

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays