Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 10:100989823 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC HM070102, CM012081

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_062_PEO1_606075_0002, 13526

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

Variation displays