Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.34 (C)
Location

Chromosome 1:39673881 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59425686

HGVS name

1:g.39673881C>T

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts and has 4292 sample genotypes.

Variant displays