Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.27 (T)
Location

Chromosome 1:116908411 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.116908411C>T

About this variant

This variant overlaps 3 transcripts and has 2506 sample genotypes.

Variant displays