Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)
Location

Chromosome 16:31315385 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

16:g.31315385C>T
ENST00000287497.10:c.1708-5856C>T
ENST00000567031.1:c.454-9014C>T
ENST00000544665.5:c.1711-5856C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays