Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.30 (G)
Location

Chromosome 12:48002667 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status

Synonyms

Archive dbSNP rs58887857, rs17119670

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

12:g.48002667G>T
ENST00000490609.1:n.250+1570C>A
ENST00000380518.5:c.85+1570C>A
ENST00000465743.2:n.501C>A
ENST00000474996.4:n.213+1570C>A
ENST00000337299.6:c.85+1570C>A

This variation has assays on 4 chips - click the plus to show

Variation displays