Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 10:74103822 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

Synonyms

LSDB VCL_2025G_A_091410

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 3 phenotypes.

Variant displays