Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

Chromosome 22:23285051 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_041885

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

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 1 citation.

Variant displays