Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)
Location

Chromosome 22:50584563 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59371778

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 2506 sample genotypes.

Variant displays