Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 6:10404795 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM101897

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003220.2:c.710G>C, 33505

This variation has 46 HGVS names - click the plus to show

Variation displays