Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59018317

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2894 sample genotypes.

Variant displays