Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 5:126192299 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57121158, rs17584016

This variation has 3 HGVS names - click the plus to show

5:g.126192299C>T
ENST00000507428.1:n.266-778C>T
ENST00000450613.2:n.71+87432G>A

This variation has assays on 6 chips - click the plus to show

Variation displays