Original source

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

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

12:g.102399791C>T
ENST00000456098.4:c.*2750G>A
ENST00000337514.9:c.*2716G>A
ENST00000626826.1:n.202207C>T

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

About this variant

This variant overlaps 7 transcripts, has 4388 individual genotypes and is mentioned in 16 citations.

Variation displays