Original source

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

Alleles
-/A
Location

Chromosome 22: between 33324261 and 33324262 (forward strand) | View in location tab

Co-located

with dbSNP rs71326530 (A/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs372619794

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

Variation displays