Original source

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

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

Chromosome 12:43778238 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14292

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 12 transcripts and is associated with 2 phenotypes.

Variant displays