Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.09 (A)
Location

Chromosome 4:73980853 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

4:g.73980853G>A

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Affy GeneChip 500K

About this variant

This variant overlaps 1 transcript and has 3824 sample genotypes.

Variant displays