Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (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
ENST00000469525.1:n.57+11535T>C
ENST00000370855.5:c.-70+11535T>C
ENST00000370859.6:c.-70+11535T>C

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 3 transcripts and has 5536 individual genotypes.

Variation displays