Original source

Variants (including SNPs and indels) imported from dbSNP (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 6 HGVS names - click the plus to show

11:g.203788C>T
ENST00000382762.3:c.*1514G>A
ENST00000410108.1:c.168+1823G>A
ENST00000526963.1:n.166C>T
ENST00000325147.9:c.*1682G>A
ENST00000433234.2:n.564G>A

This variation has assays on 8 chips - click the plus to show

Variation displays