Original source

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

G/T | Ambiguity code: K

Chromosome 19:14091875 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs11541566, rs16979459

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 11 transcripts and has 577 individual genotypes.

Variation displays