Original source

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

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

Chromosome 9:21816528 (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.21816528A>G
ENST00000419385.1:c.146-185A>G
ENST00000580900.1:c.121-185A>G
ENST00000579422.1:n.509-185A>G
ENST00000404796.2:c.121-185A>G
ENST00000380172.4:c.121-185A>G
ENST00000460874.2:c.172-185A>G
ENST00000580718.1:c.121-185A>G
ENST00000427788.2:n.507-185A>G

This variation has assays on 9 chips - click the plus to show

Variation displays