Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.06 (G)

Chromosome 7:93907514 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56649445

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 5 transcripts and has 3688 sample genotypes.

Variant displays