Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 16:56996288 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

16:g.56996288G>A
ENST00000200676.3:c.118+279G>A
ENST00000566128.1:c.-78+80G>A
ENST00000569082.1:n.116+279G>A
ENST00000379780.2:c.118+279G>A

This variation has assays on 5 chips - click the plus to show

Variation displays