Original source

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

Alleles
AA/-/A
Location

Chromosome 11:114146865-114146866 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60625868, rs71063550

This variation has 10 HGVS names - click the plus to show

Variation displays