Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.43 (T)
Location

Chromosome 12:102399791 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Hide

12:g.102399791C>T
ENST00000635615.1:n.450-23280C>T
ENST00000456098.5:c.*2750G>A
ENST00000337514.10:c.*2716G>A
ENST00000626826.1:n.202207C>T

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 8 transcripts, has 4388 sample genotypes and is mentioned in 17 citations.

Variant displays