Most severe consequence
28
intron variant
Alleles
A/G/T|Ancestral: G|MAF: 0.32 (A)|Highest population MAF: 0.49
Change tolerance
CADD: G:0.063, T:0.054|GERP: -1.84
Location
Chromosome 8:101956088 (forward strand)|VCF:8 101956088 rs993639 A G,T
Evidence status 
HGVS names
This variant has 6 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 has predicted consequences for 2 transcripts and has 3009 sample genotypes.
