Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.43 (A)
Location

Chromosome 18:22987010 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58051785, rs56514252

HGVS names

This variant has 8 HGVS names - Hide

18:g.22987010C>A
ENST00000399722.6:c.709+2020C>A
ENST00000585177.1:c.*282+2020C>A
ENST00000399721.6:c.709+2020C>A
ENST00000360790.9:c.709+2020C>A
ENST00000577445.1:c.425+2020C>A
ENST00000399725.6:c.709+2020C>A
ENST00000327155.9:c.709+2020C>A

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 8 transcripts and has 4033 sample genotypes.

Variant displays