Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.21 (C)
Location

Chromosome 17:42418584 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61051869, rs17594003

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

17:g.42418584A>C
ENST00000357037.5:c.471+4043T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Affy GeneChip 500K, Affy GenomeWideSNP_6.0

Variation displays