Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/C/T|Ancestral: G|Ambiguity code: B

Chromosome 11:2884110 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM994036, CD096712, CM096711

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 33485, 33484

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays