Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H|MAF: 0.39 (T)
Location

Chromosome 3:98816974 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1660054, rs58347474

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2766 sample genotypes.

Variant displays