Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 4:39030258 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2566092

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays