Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 11:5254939 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR850012

Most severe consequence
Evidence status

Clinical significance

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

11:g.5254939G>A
ENST00000380252.3:c.63-425C>T
ENST00000380259.4:c.-211C>T

Genotyping chips

This variation has assays on: HumanOmniExpress, Illumina_HumanOmni5

Variation displays