Original source

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

Alleles
C/T|Ambiguity code: Y|MAF: 0.43 (C)
Location

Chromosome 19:41555937 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58423993

HGVS names

This variant has 3 HGVS names - Hide

19:g.41555937C>T
ENST00000618577.4:n.35+6385C>T
ENST00000407170.6:c.-779+6385C>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 5 transcripts, has 6206 sample genotypes and is mentioned in 1 citation.

Variant displays