Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.29 (C)
Location

Chromosome 14:31954424 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

14:g.31954424A>C

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3958 sample genotypes.

Variant displays