Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2847 sample genotypes and is mentioned in 1 citation.

Variant displays