Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.41 (A)
Location

Chromosome 12:66224436 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Hide

12:g.66224436A>G
ENST00000261233.8:c.654-2287A>G
ENST00000457197.2:c.471-2287A>G

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4037 sample genotypes and is mentioned in 5 citations.

Variant displays