Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.46 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59634097, rs57185921

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

17:g.31139704G>A
ENST00000487476.2:n.444-16279G>A
ENST00000431387.5:c.61-16279G>A
ENST00000358273.5:c.61-16279G>A
ENST00000489712.3:c.-142+11197G>A
ENST00000579081.2:c.163-16279G>A
ENST00000356175.4:c.61-16279G>A
LRG_214:g.49728G>A
LRG_214t2.1:c.61-16279G>A
LRG_214t1.1:c.61-16279G>A

Genotyping chips

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

Variation displays