Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (A)
Location

Chromosome 17:48728228 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs386617571, rs3169793

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

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 3729 sample genotypes and is associated with 1 phenotype.

Variant displays