Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.38 (T)
Location

Chromosome 1:54179589 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59022236, rs56633835

HGVS names

This variant has 9 HGVS names - Hide

1:g.54179589T>C
ENST00000311841.7:c.*178+4572A>G
ENST00000534324.5:c.541-237A>G
ENST00000493530.2:c.283-237A>G
ENST00000421415.5:c.*179-237A>G
ENST00000528287.5:c.*179-237A>G
ENST00000420054.5:c.*535-237A>G
ENST00000490863.5:n.2973-237A>G
ENST00000287899.12:c.540+4572A>G

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 9 transcripts, has 4033 sample genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variant displays