Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: < 0.01 (A)
Location

Chromosome 2:46384693 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3198334

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2505 sample genotypes.

Variant displays