Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.16 (T)
Location

Chromosome 4:95492344 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58259800

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

About this variant

This variant overlaps 4 transcripts and has 3168 sample genotypes.

Variant displays