Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.34 (C)
Location

Chromosome 14:27039812 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60892220, rs17212295

This variation has 2 HGVS names - click the plus to show

14:g.27039812C>G
ENST00000552303.1:n.206-37426C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays