Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 7:44146587 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920308

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_019_GCK_138079_0005, 2203

This variation has 12 HGVS names - click the plus to show

Variation displays