Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 19:9040354 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs386504562

HGVS name

19:g.9040354C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant has 2507 sample genotypes and is mentioned in 1 citation.

Variant displays