Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

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

This variant has assays on 8 chips - click the plus to show

About this variant

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

Variant displays