Original source

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

Alleles
-/C
Location

Chromosome 10: between 114726808 and 114726809 (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