Original source

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

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

Chromosome 2:74378058 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM090400

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_004082.4:c.221A>C, 9927

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

Variation displays