Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 17:74136936 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3760134

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

17:g.74136936G>A
ENST00000585542.1:n.100+175G>A
ENST00000590137.1:n.125+175G>A
ENST00000322957.6:c.-170+259C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays