Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.32 (A)
Location

Chromosome 15:78448622 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

15:g.78448622G>A
ENST00000258886.10:c.106+8741G>A
ENST00000560454.1:n.522+8741G>A
ENST00000560840.3:c.-66+8741G>A
ENST00000559215.3:c.106+8741G>A
ENST00000560440.3:c.106+8741G>A
ENST00000558525.3:c.101+8746G>A
ENST00000558570.3:c.106+8741G>A

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

Variation displays