Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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