Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 5:150639394 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990710

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_022_GM2A_272750_0005, 17551

This variation has 7 HGVS names - click the plus to show

Variation displays