Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.42 (A)
Location

Chromosome 12:131621762 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60353831

This variation has 8 HGVS names - click the plus to show

12:g.131621762A>G
ENST00000535015.1:c.2532+203A>G
ENST00000376682.4:c.1494+203A>G
ENST00000446583.2:n.2641+203A>G
ENST00000543617.1:c.993+203A>G
ENST00000261654.5:c.2436+203A>G
ENST00000335486.6:c.497+203A>G
ENST00000540207.1:n.303+203A>G

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

Variation displays