Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2566092

This variant has 5 HGVS names - click the plus to show

About this variant

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

Variant displays