Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.05 (G)
Location

Chromosome 17:61996196 (forward strand) | View in location tab

Co-located

with dbSNP rs41318508 (C/G), rs71640270 (C/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57952803

This variation has 2 HGVS names - click the plus to show

Genotyping chips

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

Variation displays