Original source

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

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

Chromosome 10:102749028 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012073

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13530, 2010_April_001_066_PEO1_606075_0006

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

Variation displays