Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.49 (T)
Location

Chromosome 12:66224858 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17826021, rs1627870

HGVS names

This variant has 3 HGVS names - Hide

12:g.66224858T>C
ENST00000261233.8:c.654-1865T>C
ENST00000457197.2:c.471-1865T>C

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4106 sample genotypes and is mentioned in 5 citations.

Variant displays