Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.39 (T)
Location

Chromosome 19:41758692 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3795019

HGVS names

This variant has 4 HGVS names - Hide

19:g.41758692C>T
ENST00000601409.1:n.384-611G>A
ENST00000598976.1:c.425-2557C>T
ENST00000199764.6:c.424+1733C>T

About this variant

This variant overlaps 5 transcripts and has 3045 sample genotypes.

Variant displays