Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.48 (C)
Location

Chromosome 2:20689994 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs658947, rs3732142, rs60320904

This variant has 10 HGVS names - click the plus to show

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 4028 sample genotypes.

Variant displays