Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.27 (G)
Location

Chromosome 3:38723291 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17360373, rs59561525

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2541 sample genotypes and is mentioned in 1 citation.

Variant displays