Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.48 (T)
Location

Chromosome 22:41994089 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59150862

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

About this variant

This variant overlaps 12 transcripts and has 2781 sample genotypes.

Variant displays