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: 0.27 (A)
Location

Chromosome 4:6291188 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs59372792

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

4:g.6291188A>G
ENST00000507765.1:n.646-9A>G
ENST00000503569.3:c.461-9A>G
ENST00000506362.1:c.58-9A>G
ENST00000226760.3:c.461-9A>G

This variation has assays on 7 chips - click the plus to show

Variation displays