Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.14 (A)
Location

Chromosome 1:12164182 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

1:g.12164182C>A

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 3691 sample genotypes and is mentioned in 1 citation.

Variant displays