Most severe consequence
28
intron variant
Alleles
G/C/T|Ancestral: G|Highest population MAF: 0.49
Change tolerance
CADD: C:3.044, T:2.908|GERP: 0.65
Location
Chromosome 1:116925212 (forward strand)|VCF:1 116925212 rs753451 G C,T
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
This variant has 3 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 1 transcript and has 3009 sample genotypes.