Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.16 (G)
Location

Chromosome 4:39009696 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2507 sample genotypes.

Variant displays