Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (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
ENST00000413302.4:c.*1576T>C

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

Variation displays