Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 16:176756 (forward strand) | View in location tab
with PhenCode HbVar.2796 (G/A)
This variation has 3 synonyms - click the plus to show
This variation has 12 HGVS names - click the plus to show
This variant overlaps 21 transcripts.