Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.24 (A)

Chromosome 14:103706470 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 11 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 4116 individual genotypes and is mentioned in 2 citations.

Variation displays