Original source

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

GATTC/- | MAF: 0.37 (GATTC)

Chromosome 11:18401458-18401462 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

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

About this variant

This variant overlaps 26 transcripts and has 2504 sample genotypes.

Variant displays