Original source

Variants (including SNPs and indels) imported from dbSNP (release 139)|View in dbSNP

Alleles
C/T|Ambiguity code: Y
Location

Chromosome 35:10274 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Synonyms

Archive dbSNP rs8281648

HGVS name

35:g.10274C>T

Variant displays