Original source

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

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

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

Most severe consequence
Evidence status


Archive dbSNP rs586301

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2507 individual genotypes.

Variation displays