Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.11 (A)
Location

Chromosome 4:89775676 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59018317

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2894 individual genotypes.

Variation displays