Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.03 (C)
Location

Chromosome 18:22171187 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_067380

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 15 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays