Original source

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

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

Chromosome 16:23635076 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_024675.3:c.1470C>T

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays