Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:16991749 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM085956

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_058458

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays