Original source

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

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

Chromosome 7:44189362 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970636

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB GCK_676G_A_060311

This variation has 9 HGVS names - click the plus to show

Variation displays