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: 0.25 (A)
Location

Chromosome 16:68787043 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59368541

This variation has 13 HGVS names - click the plus to show

16:g.68787043G>A
ENST00000611625.2:c.164-14627G>A
ENST00000612417.2:c.164-14627G>A
ENST00000564676.3:n.446-14627G>A
ENST00000566612.3:c.164-14627G>A
ENST00000422392.4:c.164-14627G>A
ENST00000621016.2:c.164-14627G>A
ENST00000564745.1:n.159-14627G>A
ENST00000261769.7:c.164-14627G>A
ENST00000566510.3:c.164-14627G>A
ENST00000562836.3:n.235-14627G>A
LRG_301:g.54752G>A
LRG_301t1:c.164-14627G>A

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

Variation displays