Original source

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

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

Chromosome 16:58521649 (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.58521649T>A
ENST00000569924.1:n.337-332A>T
ENST00000317147.7:c.6918-332A>T
ENST00000569240.3:c.6903-332A>T
ENST00000245138.6:c.932-332A>T
ENST00000567188.3:c.*633-332A>T
ENST00000563130.3:n.1793-332A>T

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

Variation displays