Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.47 (G)
Location

Chromosome 1:109571989 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1279339

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2776 sample genotypes.

Variant displays