Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 7:94627959 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59328897

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2903 individual genotypes.

Variation displays