Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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