Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.24 (G)
Location

Chromosome 4:54671315 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17232766, rs3796766

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 4 transcripts, has 3765 sample genotypes and is mentioned in 1 citation.

Variant displays