Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

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

15:g.78448622G>A
ENST00000258886.12:c.106+8741G>A
ENST00000560454.1:n.522+8741G>A
ENST00000560840.5:c.-66+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

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

About this variant

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

Variant displays