Original source

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

Alleles
T/G | Ambiguity code: K | MAF: 0.47 (T)
Location

Chromosome 19:44905579 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR982405

Most severe consequence
 
Upstream gene variant
Evidence status

Clinical significance

Synonyms
HGVS name

19:g.44905579T>G

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 3695 sample genotypes, is associated with 4 phenotypes and is mentioned in 66 citations.

Variant displays