Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.19 (G)
Location

Chromosome 1:75599505 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17304008

This variation has 4 HGVS names - click the plus to show

1:g.75599505A>G
ENST00000370855.5:c.-70+11535T>C
ENST00000469525.1:n.57+11535T>C
ENST00000370859.5:c.-70+11535T>C

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays