Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 4:47032412 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays