Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.24 (T)
Location

Chromosome 16:68799040 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58580657, rs17690402

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

16:g.68799040C>T
ENST00000611625.2:c.164-2630C>T
ENST00000564676.3:n.446-2630C>T
ENST00000612417.2:c.164-2630C>T
ENST00000566612.3:c.164-2630C>T
ENST00000621016.2:c.164-2630C>T
ENST00000422392.4:c.164-2630C>T
ENST00000261769.7:c.164-2630C>T
ENST00000564745.1:n.159-2630C>T
ENST00000566510.3:c.164-2630C>T
ENST00000562836.3:n.235-2630C>T
LRG_301:g.66749C>T
LRG_301t1:c.164-2630C>T

This variation has assays on 9 chips - click the plus to show

Variation displays