Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.34 (A)
Location

Chromosome 17:43044391 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3169715, rs59800937

This variant has 5 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 3844 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays