Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.23 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57230811

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

15:g.78482334A>G
ENST00000258886.11:c.1297-984A>G
ENST00000558570.4:c.*564-984A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 1175 individual genotypes and is mentioned in 5 citations.

Variation displays