Original source

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

Alleles
C/T | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:14091568 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

19:g.14091568C>T

About this variant

Variant displays