Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 2:234180410 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57980349, rs61379225

This variation has 13 HGVS names - click the plus to show

2:g.234180410A>G
ENST00000373525.5:c.276-1202A>G
ENST00000392017.4:c.708-1202A>G
ENST00000444735.1:c.276-1202A>G
ENST00000474148.1:n.835-1202A>G
ENST00000392021.3:c.*589-1202A>G
ENST00000479942.1:n.854-1202A>G
ENST00000498620.1:n.272-1202A>G
ENST00000392020.4:c.708-1202A>G
ENST00000419681.1:c.276-1202A>G
ENST00000347464.5:c.276-1202A>G
ENST00000417017.1:c.456-1202A>G
ENST00000392018.1:c.708-1202A>G

This variation has assays on 6 chips - click the plus to show

Variation displays