Original source

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

AAAC/- | MAF: 0.37 (AAAC)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs148072862, rs143718787

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

About this variant

This variant overlaps 23 transcripts and has 2513 sample genotypes.

Variant displays