Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 20:9073048 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17753214, rs56848719

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

About this variant

This variant overlaps 4 transcripts and has 4876 individual genotypes.

Variation displays