Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 17:4899390 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

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

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays