Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.50 (A)
Location

Chromosome 17:31139704 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59634097, rs57185921

This variant has 10 HGVS names - click the plus to show

17:g.31139704G>A
ENST00000487476.5:n.444-16279G>A
ENST00000431387.8:c.61-16279G>A
ENST00000358273.8:c.61-16279G>A
ENST00000489712.6:c.-142+11197G>A
ENST00000579081.5:c.163-16279G>A
ENST00000356175.7:c.61-16279G>A
LRG_214:g.49728G>A
LRG_214t2:c.61-16279G>A
LRG_214t1:c.61-16279G>A

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 9 transcripts and has 3448 sample genotypes.

Variant displays