Original source

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

AAAC/- | MAF: 0.36 (AAAC)

Chromosome 11:18405840-18405843 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs148072862, rs143718787

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

About this variant

This variant overlaps 23 transcripts and has 1101 individual genotypes.

Variation displays