Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.34 (G)
Location

Chromosome 17:38975328 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT10:c.1459C>T (A/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays