Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.13 (T)
Location

Chromosome 1:116908876 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59907887

HGVS name

1:g.116908876C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3763 sample genotypes.

Variant displays