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 7:44147732 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920306

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2202, 2010_April_001_018_GCK_138079_0004

This variation has 11 HGVS names - click the plus to show

Variation displays