Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:5276169 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR850012

Most severe consequence
Evidence status

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

11:g.5276169G>A
ENST00000380252.1:c.63-425C>T
ENST00000380259.2:c.-211C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays