Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.44 (T)
Location

Chromosome 17:47573690 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 26 HGVS names - click the plus to show

Variation displays