Original source

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

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

Chromosome 19:45419208 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB Broad13929284

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 17 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays