Original source

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

Alleles
C/G | Ambiguity code: S
Location

Chromosome 22:23314599 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_041896

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays