Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: < 0.01 (T)
Location

Chromosome 9:37429981 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.598+145G>T

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays