Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.31 (G)
Location

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

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs58887857, rs17119670

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

12:g.48002667G>T
ENST00000490609.1:n.250+1570C>A
ENST00000380518.7:c.85+1570C>A
ENST00000465743.2:n.501C>A
ENST00000337299.6:c.85+1570C>A
ENST00000474996.6:n.213+1570C>A

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2744 sample genotypes and is mentioned in 2 citations.

Variant displays