Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 9:21816529 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17760747, rs58101861

This variation has 9 HGVS names - click the plus to show

9:g.21816529A>G
ENST00000419385.2:c.146-185A>G
ENST00000580900.2:c.121-185A>G
ENST00000579422.2:n.509-185A>G
ENST00000404796.2:c.121-185A>G
ENST00000380172.5:c.121-185A>G
ENST00000460874.3:c.172-185A>G
ENST00000580718.1:c.121-185A>G
ENST00000427788.2:n.507-185A>G

This variation has assays on 10 chips - click the plus to show

Variation displays