Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 1:16988161 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM098012

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_058461

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays