Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome 10:81883883 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

10:g.81883883C>G
ENST00000555784.2:c.135+5788C>G
ENST00000602794.2:c.61-5307C>G
ENST00000404576.3:c.135+5788C>G
ENST00000404547.2:c.823+7720C>G
ENST00000556918.2:c.135+5788C>G
ENST00000372142.3:c.60+5863C>G
ENST00000372141.3:c.823+7720C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays