Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 9:37428599 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.493+27C>T

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays