Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.45 (T)
Location

Chromosome 5:150899025 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58698195

This variant has 7 HGVS names - click the plus to show

5:g.150899025C>T
ENST00000427179.5:c.16-471G>A
ENST00000418587.6:c.-93-471G>A
ENST00000394226.2:c.16-471G>A
ENST00000274599.9:c.16-471G>A
ENST00000446148.6:c.64-471G>A
ENST00000520549.1:c.*141-1564C>T

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2615 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays