Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.25 (C)
Location

Chromosome 17:17224603 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs57331099

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2511 sample genotypes.

Variant displays