Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.12 (G)
Location

Chromosome 14:91180065 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

14:g.91180065A>G
ENST00000557766.1:c.393-14498T>C
ENST00000328459.6:c.698+16354T>C
ENST00000357056.2:c.698+16354T>C

This variation has assays on 4 chips - click the plus to show

Variation displays