Original source

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

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

Chromosome 1:206771300 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3748675

HGVS names

This variant has 2 HGVS names - Hide

1:g.206771300T>C
ENST00000423557.1:c.225+56A>G

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3807 sample genotypes, is associated with 1 phenotype and is mentioned in 22 citations.

Variant displays