Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17594003, rs61051869

HGVS names

This variant has 2 HGVS names - Hide

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

Genotyping chips

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

About this variant

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

Variant displays