Original source

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

Alleles
-/CA
Location

Chromosome 4: between 146641871 and 146641872 (forward strand) | View in location tab

Most severe consequence

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

Variation displays