Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.44 (C)
Location

Chromosome 6:43997428 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57503978

HGVS names

This variant has 3 HGVS names - Hide

6:g.43997428T>C
ENST00000422059.5:n.647-120A>G
ENST00000607590.1:n.430-120A>G

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3691 sample genotypes and is mentioned in 1 citation.

Variant displays