Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.47 (T)
Location

Chromosome 16:88643329 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR995275

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17701020, rs3189363

HGVS names

This variant has 4 HGVS names - Hide

16:g.88643329C>T
ENST00000261623.7:c.*24G>A
LRG_52:g.12721G>A
LRG_52t1:c.*24G>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 13 transcripts, has 3759 sample genotypes and is mentioned in 8 citations.

Variant displays