Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

T/C | Ambiguity code: Y | MAF: 0.23 (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 1099 individual genotypes.

Variation displays