Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.36 (G)
Location

Chromosome 5:159315942 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR025273

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Hide

5:g.159315942T>G
ENST00000521472.5:n.289+4528T>G
ENST00000231228.2:c.*159A>C
LRG_71:g.19532A>C
LRG_71t1:c.*159A>C

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4338 sample genotypes and is mentioned in 126 citations.

Variant displays