Original source

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

Alleles
A/C/G|Ancestral: G|Ambiguity code: V|MAF: 0.45 (A)
Location

Chromosome 19:45937042 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs59992602, rs17652042

HGVS names

This variant has 4 HGVS names - Hide

Variant allele C
19:g.45937042A>C
ENST00000263257.5:c.*2821T>G

Variant allele G
19:g.45937042A>G
ENST00000263257.5:c.*2821T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3762 sample genotypes and is mentioned in 1 citation.

Variant displays