Original source

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

HGVS names

This variant has 4 HGVS names - Hide

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

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

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

Variant displays