Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.42 (C)
Location

Chromosome 9:133643810 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59265623

This variation has 2 HGVS names - click the plus to show

9:g.133643810G>C
ENST00000393056.3:c.921+221G>C

Variation displays