Original source

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

Alleles
-/CC/TC
Location

Chromosome 4: between 9779768 and 9779769 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs367729020

This variation has 4 HGVS names - click the plus to show

Variation displays