Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.22 (C)

Chromosome 4:54101047 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386603483, rs60588190

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3691 sample genotypes.

Variant displays