Original source

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

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

Chromosome 4:54228348 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1800811

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, 2 regulatory features, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays