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: 0.50 (T)
Location

Chromosome 2:60493111 (forward strand) | View in location tab

Co-located
Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs58246907

This variation has 8 HGVS names - click the plus to show

2:g.60493111C>T
ENST00000356842.6:c.386-24278G>A
ENST00000492272.3:n.228-24278G>A
ENST00000335712.8:c.386-24278G>A
ENST00000358510.4:c.386-30687G>A
ENST00000489516.4:n.378-24278G>A
ENST00000359629.7:c.386-24278G>A
ENST00000477659.1:n.69-24278G>A

This variation has assays on 7 chips - click the plus to show

Variation displays