Original source

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

Alleles
-/C
Location

Chromosome 10: between 112967049 and 112967050 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144667283

This variation has 14 HGVS names - click the plus to show

Variation displays