Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.27 (T)
Location

Chromosome 16:79066662 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

16:g.79066662A>T
ENST00000406884.3:c.517-144946A>T
ENST00000539474.3:c.486-144946A>T
ENST00000566780.2:c.1057-144946A>T
ENST00000569332.2:c.*854-144946A>T
ENST00000402655.3:c.410-144946A>T

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

Variation displays