Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 5:125527992 (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.125527992C>T
ENST00000507428.1:n.266-778C>T
ENST00000450613.2:n.71+87431G>A

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

Variation displays