Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.10 (A)
Location

Chromosome 14:22465666 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 7 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 4029 individual genotypes.

Variation displays