Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.34 (A)
Location

Chromosome 5:256357 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 2510 individual genotypes and is associated with 1 phenotype.

Variation displays