Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.31 (C)

Chromosome 4:25360496 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2671446

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 4 transcripts and has 3694 sample genotypes.

Variant displays