Most severe consequence
28
intron variant
Alleles
C/G/T|Ancestral: C|MAF: 0.38 (T)|Highest population MAF: 0.49
Change tolerance
CADD: G:8.181, T:8.532|GERP: 0.71
Location
Chromosome 8:101975145 (forward strand)|VCF:8 101975145 rs4734044 C 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.
