Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.41 (T)
Location

Chromosome 9:35079364 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs59950148, rs17879660

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 4106 sample genotypes and is mentioned in 1 citation.

Variant displays