Original source

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

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

Chromosome 12:131137217 (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.131137217A>G
ENST00000376682.6:n.1749+203A>G
ENST00000535015.3:c.2532+203A>G
ENST00000446583.4:c.786+203A>G
ENST00000543617.2:c.993+203A>G
ENST00000261654.7:c.2436+203A>G
ENST00000335486.8:c.282+203A>G
ENST00000540207.1:n.303+203A>G

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

Variation displays