Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:116835994 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD072343

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variation displays