Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs57041342

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

22:g.21028193T>C
ENST00000413302.5:c.*1576T>C

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 3689 individual genotypes.

Variation displays