Most severe consequence
28
intron variant
Alleles
C/G/T|Ancestral: C|MAF: 0.16 (T)|Highest population MAF: 0.44
Change tolerance
CADD: G:0.449, T:0.573|GERP: -3.00
Location
Chromosome 5:37829283 (forward strand)|VCF:5 37829283 rs2910701 C G,T
Evidence status 
HGVS names
This variant has 4 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 1 transcript and has 3009 sample genotypes.
