Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 17:43124125 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB U14680.1:c.-19-10T>C

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 27 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays