Original source

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

A/G/T | Ancestral: G | Ambiguity code: D | MAF: 0.41 (A)

Chromosome 11:18402940 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 50 transcripts and has 1145 individual genotypes.

Variation displays