Original source

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

G/-/GATTC | Ancestral: G

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

Most severe consequence
Evidence status


Archive dbSNP rs147366647, rs111514460

This variation has 34 HGVS names - click the plus to show

About this variant

This variant overlaps 52 transcripts and has 1 individual genotype.

Variation displays