Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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