Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

Chromosome 3:46902303 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014210

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 15 HGVS names - click the plus to show

Variation displays