Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 1:236755183 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2539 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays