Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.43 (T)
Location

Chromosome 3:41200876 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2371451

HGVS names

This variant has 10 HGVS names - Show

About this variant

Variant displays