Most severe consequence
28
intron variant
Alleles
C/T|Ancestral: C|MAF: 0.28 (T)|Highest population MAF: 0.46
Change tolerance
CADD: T:6.976|GERP: -3.91
Location
Chromosome 5:52932612 (forward strand)|VCF:5 52932612 rs10513003 C T
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Synonyms
ClinGen Allele Registry CA15419717 (T)
Genotyping chips
This variant has assays on: Illumina_HumanOmni5, Illumina_HumanOmni2.5
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 2 transcripts, has 3009 sample genotypes and is mentioned in 2 citations.
