Most severe consequence
28
intron variant
Alleles
C/A/G/T|Ancestral: C|Highest population MAF: 0.44
Change tolerance
CADD: A:1.933, G:2.018, T:3.626|GERP: -3.86
Location
Chromosome 22:18914365 (forward strand)|VCF:22 18914365 rs395440 C A,G,T
Evidence status 
HGVS names
This variant has 12 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 3 transcripts and has 2504 sample genotypes.
