Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.03 (C)
Location

Chromosome 1:156814582 (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 7 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2504 individual genotypes.

Variation displays