Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 12:131137217 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60353831

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

12:g.131137217A>G
ENST00000535015.5:c.2532+203A>G
ENST00000543617.2:c.993+203A>G
ENST00000376682.8:n.1749+203A>G
ENST00000446583.6:c.786+203A>G
ENST00000261654.9:c.2436+203A>G
ENST00000335486.10:c.282+203A>G
ENST00000540207.1:n.303+203A>G

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

About this variant

This variant overlaps 8 transcripts, has 3964 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays