Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.31 (A)
Location

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Hide

15:g.78448622G>A
ENST00000560840.5:c.-66+8741G>A
ENST00000258886.12:c.106+8741G>A
ENST00000560454.1:n.522+8741G>A
ENST00000559215.5:c.106+8741G>A
ENST00000560440.5:c.106+8741G>A
ENST00000558525.5:c.101+8746G>A
ENST00000558570.5:c.106+8741G>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3762 sample genotypes and is mentioned in 9 citations.

Variant displays