Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

Synonyms

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

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2504 sample genotypes.

Variant displays