Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 10:100989165 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050079

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_021830.3:c.955A>G, 13534, 2010_April_001_070_PEO1_606075_0010

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

Variation displays