Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Hide

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