Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 22:51064081 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940110

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 34 HGVS names - click the plus to show

Variation displays