Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 10:102749073 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023775

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13533, 2010_April_001_069_PEO1_606075_0009

This variation has 16 HGVS names - click the plus to show

Variation displays