Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

AT/- | MAF: 0.04 (-)

Chromosome 18:5405835-5405836 (forward strand) | View in location tab

Most severe consequence

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 1092 individual genotypes.

Variation displays