Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 16:226744 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086364 ; PhenCode HbVar.2594 (A/G) ; dbSNP rs35836455 (A/C)

Most severe consequence

This variation has 2 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Variation displays