Original source

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

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

Chromosome 3:183822955 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs7427372

HGVS names

This variant has 5 HGVS names - Hide

3:g.183822955T>C
ENST00000463801.1:n.79+2192A>G
ENST00000431348.1:c.401+2192A>G
ENST00000318631.7:c.401+2192A>G
ENST00000445426.1:c.375+2192A>G

About this variant

Variant displays