Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.23 (T)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17690402, rs58580657

HGVS names

This variant has 13 HGVS names - Hide

16:g.68799040C>T
ENST00000611625.4:c.164-2630C>T
ENST00000612417.4:c.164-2630C>T
ENST00000564676.5:n.446-2630C>T
ENST00000566612.5:c.164-2630C>T
ENST00000422392.6:c.164-2630C>T
ENST00000621016.4:c.164-2630C>T
ENST00000564745.1:n.159-2630C>T
ENST00000261769.9:c.164-2630C>T
ENST00000566510.5:c.164-2630C>T
ENST00000562836.5:n.235-2630C>T
LRG_301:g.66749C>T
LRG_301t1:c.164-2630C>T

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature, has 4033 sample genotypes and is mentioned in 8 citations.

Variant displays