Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.24 (G)
Location

Chromosome 17:31203691 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs55794969, rs61071686

This variant has 11 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 3804 sample genotypes.

Variant displays