Original source

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