Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.02 (G)
Location

Chromosome 14:101962919 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

14:g.101962919A>G

About this variant

This variant overlaps 1 transcript and has 2594 sample genotypes.

Variant displays