Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.35 (A)
Location

Chromosome 1:62837115 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17388534

This variation has 3 HGVS names - click the plus to show

1:g.62837115A>G
ENST00000317868.5:c.1089+2263A>G
ENST00000371120.4:c.1089+2263A>G

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays