Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome 9:35096109 (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 13 transcripts and has 2505 individual genotypes.

Variation displays