Original source

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

Synonyms

LSDB VCL_2025G_A_091410

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays