Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.45 (A)
Location

Chromosome 4:94993082 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58574150, rs4091830

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2508 individual genotypes.

Variation displays