Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 5:150278587 (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.150278587C>T
ENST00000427179.1:c.16-471G>A
ENST00000418587.2:c.-93-471G>A
ENST00000274599.5:c.16-471G>A
ENST00000394226.2:c.16-471G>A
ENST00000446148.2:c.64-471G>A
ENST00000520549.1:c.*141-1564C>T

This variation has assays on 6 chips - click the plus to show

Variation displays