Most severe consequence
38
Intergenic variant
Alleles
C/T
Location
Chromosome 35:10274 (forward strand)|View in location tab
Co-located variant
dbSNP rs852034667 (C/T)
HGVS name
NC_006617.3:g.10274C>T
Synonyms
Archive dbSNP rs8281648
Original source
Variants (including SNPs and indels) imported from dbSNP (release 146)|View in dbSNP
