Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 11:89011046 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17800907, rs56750720

This variation has 2 HGVS names - click the plus to show

11:g.89011046G>A
ENST00000263321.5:c.1185-6895G>A

This variation has assays on 12 chips - click the plus to show

Variation displays