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 7:44184770 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980898

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2207, 2010_April_001_022_GCK_138079_0009

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

Variation displays