Original source

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

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

Chromosome 17:61995262 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_011918

This variation has 10 HGVS names - click the plus to show

Genotyping chips

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

Variation displays