Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.03 (T)
Location

Chromosome 14:77786864 (forward strand) | View in location tab

Co-located

with PhenCode POMT2:c.161C>A (G/T)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_022083

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5

Variation displays