Original source

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

T/C/G | Ancestral: C | Ambiguity code: B | MAF: 0.11 (T)

Chromosome 19:17403506 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs12984092, rs117201450

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 2507 sample genotypes.

Variant displays