Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (A)
Location

Chromosome 4:6292915 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59372792

This variation has 5 HGVS names - click the plus to show

4:g.6292915A>G
ENST00000507765.1:n.646-9A>G
ENST00000503569.1:c.461-9A>G
ENST00000506362.1:c.58-9A>G
ENST00000226760.1:c.461-9A>G

This variation has assays on 5 chips - click the plus to show

Variation displays