Original source

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

ACAAA/- | MAF: 0.27 (-)

Chromosome 16:50752262-50752266 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs151087977

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 1096 individual genotypes.

Variation displays