Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.27 (G)
Location

Chromosome 15:78482334 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57230811

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

15:g.78482334A>G
ENST00000258886.12:c.1297-984A>G
ENST00000558570.5:c.*564-984A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2579 sample genotypes and is mentioned in 5 citations.

Variant displays