Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 4 HGVS names - click the plus to show

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

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

This variant has assays on 9 chips - click the plus to show

About this variant

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

Variant displays