Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.05 (G)
Location

Chromosome 17:63918647 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2766 individual genotypes and is mentioned in 2 citations.

Variation displays