Original source

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

AAAG/- | MAF: 0.24 (AAAG)

Chromosome 5:96775265-96775268 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 24 transcripts and has 1099 individual genotypes.

Variation displays