Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.08 (G)
Location

Chromosome 5:159315006 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2940 individual genotypes and is mentioned in 3 citations.

Variation displays