Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (T)
Location

Chromosome 19:30289289 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60808716, rs12982313

This variant has 4 HGVS names - click the plus to show

19:g.30289289T>C
ENST00000591488.1:c.-120+60616T>C
ENST00000585628.5:c.-120+5148T>C
ENST00000590564.5:n.454+5148T>C

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 3959 sample genotypes and is mentioned in 1 citation.

Variant displays