Original source

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

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

About this variant

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

Variant displays