Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.37 (A)
Location

Chromosome 14:100824126 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts, has 2772 sample genotypes and is mentioned in 1 citation.

Variant displays