Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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