Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.09 (A)
Location

Chromosome 2:208122114 (forward strand) | View in location tab

Co-located

with dbSNP rs202160884 (C/-)

Most severe consequence
 
Intron variant
Evidence status

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

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays