Most severe consequence
28
intron variant
Alleles
A/C/G/T|Ancestral: A|Highest population MAF: 0.38
Change tolerance
CADD: C:8.299, G:8.568, T:8.258|GERP: -2.38
Location
Chromosome 8:102023715 (forward strand)|VCF:8 102023715 rs1269714 A C,G,T
Co-located variant
dbSNP rs1822358982 (A/-)
Evidence status 
HGVS names
This variant has 9 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 2 transcripts, 1 regulatory feature and has 3009 sample genotypes.
