Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs4350811

HGVS name

20:g.45919554C>T

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2510 individual genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays