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: 0.49 (C)
Location

Chromosome 4:88962828 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59688598

This variation has 6 HGVS names - click the plus to show

4:g.88962828C>T
ENST00000511976.2:c.-22-24587G>A
ENST00000509094.2:c.606-24587G>A
ENST00000512339.2:c.428-24587G>A
ENST00000264344.6:c.606-24587G>A
ENST00000502459.2:n.1064-24587G>A

This variation has assays on 10 chips - click the plus to show

Variation displays