Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.46 (A)
Location

Chromosome 16:58555553 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59662370, rs59076330

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

16:g.58555553T>A
ENST00000317147.5:c.6918-332A>T
ENST00000569924.1:n.337-332A>T
ENST00000569240.1:c.6903-332A>T
ENST00000245138.4:c.3471-332A>T
ENST00000567188.1:c.*633-332A>T
ENST00000563130.1:n.1793-332A>T

This variation has assays on 4 chips - click the plus to show

Variation displays