Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G/T | Ambiguity code: D | MAF: 0.37 (A)

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

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 48 HGVS names - Show

About this variant

This variant overlaps 50 transcripts and has 2545 sample genotypes.

Variant displays