Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.38 (G)
Location

Chromosome 12:40197315 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Hide

12:g.40197315A>G
ENST00000416796.5:c.-63+542A>G
ENST00000412812.1:n.146-6921T>C

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3762 sample genotypes and is mentioned in 3 citations.

Variant displays