Original source

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

T/C | Ambiguity code: Y | MAF: 0.26 (C)

Chromosome 19:11386305 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs586301

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2507 sample genotypes.

Variant displays