Original source

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

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

Chromosome 1:17314656 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM098012

Most severe consequence
Evidence status

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