Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.22 (C)

Chromosome 4:89776006 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17796248

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, has 2570 sample genotypes and is mentioned in 1 citation.

Variant displays