Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 4:167112653 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59362509

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 2782 sample genotypes.

Variant displays