Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: < 0.01 (G)
Location

Chromosome 1:2226752 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.2226752C>G

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays