Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.30 (A)
Location

Chromosome 12:47995860 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59687871

This variation has 3 HGVS names - click the plus to show

12:g.47995860A>C
ENST00000380518.4:c.654+15T>G
ENST00000337299.6:c.447+15T>G

This variation has assays on 11 chips - click the plus to show

Variation displays