Original source

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

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

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

Most severe consequence
Splice region variant
Evidence status

Clinical significance


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