Most severe consequence
38
Intergenic variant
Alleles
C/T|Highest population MAF: 0.26
Location
Chromosome 18:64264731 (forward strand)|View in location tab
Evidence status 
HGVS name
NC_019475.1:g.64264731C>T
Synonyms
Archive dbSNP rs10721220
Original source
Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP
About this variant
This variant has 177 sample genotypes.
