Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:237589784 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 5 sample genotypes and is associated with 2 phenotypes.

Variant displays