Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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