Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 2:74378068 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM090396

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_004082.4:c.211G>A, 9926

This variation has 27 HGVS names - click the plus to show

Variation displays