This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: 0.08 (A)
Location

Chromosome 19:41332301 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60826558

HGVS names

This variant has 12 HGVS names - Hide

Variant allele A
19:g.41332301G>A
ENST00000221930.5:c.861-20C>T
ENST00000600196.1:n.173-20C>T
ENST00000598758.5:c.149-20C>T

Variant allele T
19:g.41332301G>T
ENST00000221930.5:c.861-20C>A
ENST00000600196.1:n.173-20C>A
ENST00000598758.5:c.149-20C>A

Variant allele C
19:g.41332301G>C
ENST00000221930.5:c.861-20C>G
ENST00000600196.1:n.173-20C>G
ENST00000598758.5:c.149-20C>G

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3562 sample genotypes and is mentioned in 17 citations.

Variant displays