Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.33 (C)
Location

Chromosome 22:21028193 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs57041342

HGVS names

This variant has 2 HGVS names - Hide

22:g.21028193T>C
ENST00000413302.6:c.*1576T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3689 sample genotypes and is associated with 1 phenotype.

Variant displays