Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2509 sample genotypes.

Variant displays