Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.03 (G)
Location

Chromosome 1:153259362 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs111764845

HGVS name

1:g.153259362C>G

About this variant

This variant overlaps 1 transcript and has 2506 sample genotypes.

Variant displays