Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.24 (A)
Location

Chromosome 11:68855363 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM083200

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

11:g.68855363G>A
ENST00000542467.1:c.1655G>A
ENSP00000445551.1:p.Gly552Glu
ENST00000442692.2:n.1667G>A
ENST00000294309.3:c.2201G>A
ENSP00000294309.3:p.Gly734Glu

This variation has assays on 9 chips - click the plus to show

Variation displays