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 1:43805713 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002060

Most severe consequence
Clinical significance

Synonyms

LSDB 4167

This variation has 8 HGVS names - click the plus to show

Variation displays