Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.34 (C)
Location

Chromosome 2:44313102 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59596751, rs17607686

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 3122 sample genotypes.

Variant displays