Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.06 (T)
Location

Chromosome 1:39903005 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.39903005A>T

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays