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
ENST00000611625.1:c.164-14627G>A
ENST00000612417.1:c.164-14627G>A
ENST00000564676.2:n.446-14627G>A
ENST00000566612.2:c.164-14627G>A
ENST00000422392.3:c.164-14627G>A
ENST00000621016.1:c.164-14627G>A
ENST00000564745.1:n.159-14627G>A
ENST00000261769.6:c.164-14627G>A
ENST00000566510.2:c.164-14627G>A
ENST00000562836.2:n.235-14627G>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