Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 11:203788 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117234720, rs58518031

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

11:g.203788C>T
ENST00000382762.5:c.*1514G>A
ENST00000410108.3:c.168+1823G>A
ENST00000526963.1:n.166C>T
ENST00000325147.11:c.*1682G>A

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

Variation displays