Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 17:63917902 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_011918

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 7 transcripts and has 267 individual genotypes.

Variation displays