Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.12 (C)
Location

Chromosome 2:207552876 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61490155

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2509 sample genotypes.

Variant displays