Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ambiguity code: Y | MAF: 0.42 (T)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58698195

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

5:g.150899025C>T
ENST00000418587.5:c.-93-471G>A
ENST00000427179.4:c.16-471G>A
ENST00000394226.2:c.16-471G>A
ENST00000274599.8:c.16-471G>A
ENST00000446148.5:c.64-471G>A
ENST00000520549.1:c.*141-1564C>T

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

About this variant

This variant overlaps 6 transcripts, has 2281 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays