Original source

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

Alleles
-/G
Location

Chromosome 16: between 23365620 and 23365621 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs149626590, rs59922401

This variation has 7 HGVS names - click the plus to show

Variation displays