Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 16:68820946 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59368541

This variation has 10 HGVS names - click the plus to show

16:g.68820946G>A
ENST00000566612.1:c.164-14627G>A
ENST00000422392.2:c.164-14627G>A
ENST00000261769.5:c.164-14627G>A
ENST00000564745.1:n.159-14627G>A
ENST00000566510.1:c.164-14627G>A
ENST00000562836.1:n.235-14627G>A
ENST00000564676.1:n.446-14627G>A
LRG_301:g.54752G>A
LRG_301t1.1:c.164-14627G>A

This variation has assays on 8 chips - click the plus to show

Variation displays