Most severe consequence
28
intron variant
Alleles
T/A/C/G|Ancestral: C|MAF: 0.47 (C)|Highest population MAF: 0.50
Change tolerance
CADD: A:2.059, C:2.462, G:2.126|GERP: -3.74
Location
Chromosome 8:101942164 (forward strand)|VCF:8 101942164 rs11778653 T A,C,G
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 and has 3009 sample genotypes.
