Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.24 (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: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript, has 4038 individual genotypes and is mentioned in 5 citations.

Variation displays