Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.10 (G)
Location

Chromosome 2:227815621 (forward strand) | View in location tab

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

Synonyms

Archive dbSNP rs60930044

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2847 individual genotypes.

Variation displays