Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (G)
Location

Chromosome 3:89306482 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57189474

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2508 individual genotypes.

Variation displays