Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.31 (T)
Location

Chromosome 20:45919554 (forward strand)|View in location tab

Most severe consequence
 
Regulatory region variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS name

20:g.45919554C>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 2510 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays