Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 12:66209619 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

12:g.66209619C>T
ENST00000261233.8:c.381+99C>T
ENST00000457197.2:c.198+99C>T

About this variant

This variant overlaps 2 transcripts, has 2556 sample genotypes and is mentioned in 4 citations.

Variant displays